NDC Code(s) : 0573-0165-20, 0573-0165-30, 0573-0165-40, 0573-0165-41, 0573-0165-42, 0573-0165-31, 0573-0165-25, 0573-0154-35, 0573-0154-75, 0573-0154-17, 0573-0154-89, 0573-0154-84, 0573-0154-98, 0573-0154-16, 0573-0154-60, 0573-0154-59, 0573-0154-21, 0573-0151-12, 0573-0151-13, 0573-0151-10, 0573-0151-21, 0573-0151-20, 0573-0151-48, 0573-0151-30, 0573-0151-05, 0573-0161-35, 0573-0161-51, 0573-0161-85, 0573-0161-65, 0573-0166-51, 0573-0166-85, 0573-0150-20, 0573-0150-30, 0573-0150-40, 0573-0150-31, 0573-0150-32, 0573-0150-41, 0573-0150-42, 0573-0160-20, 0573-0160-30, 0573-0160-40, 0573-0160-25, 0573-0160-31, 0573-0160-41, 0573-0160-42, 0573-0160-17, 0573-1711-14
Packager : Haleon US Holdings LLC

Category : HUMAN OTC DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0165
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FD&C RED NO. 40(UNII: WZB9127XOA)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
FERRIC OXIDE RED(UNII: 1K09F3G675)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
GLYCERIN(UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED(UNII: 3NXW29V3WO)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
PROPYL GALLATE(UNII: 8D4SNN7V92)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
TRIACETIN(UNII: XHX3C3X673)
WATER(UNII: 059QF0KO0R)
Product Characteristics
Color brown (one side is brown while the other side is yellow) Score no score
Shape OVAL Size 16 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0165-201 in 1 CARTON 18/05/1984
124 in 1 BOTTLE Type 0: Not a Combination Product
2NDC:0573-0165-301 in 1 CARTON 18/05/1984
250 in 1 BOTTLE Type 0: Not a Combination Product
3NDC:0573-0165-401 in 1 CARTON 18/05/1984
3100 in 1 BOTTLE Type 0: Not a Combination Product
4NDC:0573-0165-411 in 1 CARTON 18/05/1984
4125 in 1 BOTTLE Type 0: Not a Combination Product
5NDC:0573-0165-421 in 1 CARTON 18/05/1984
5150 in 1 BOTTLE Type 0: Not a Combination Product
6NDC:0573-0165-311 in 1 CARTON 18/05/1984
675 in 1 BOTTLE Type 0: Not a Combination Product
7NDC:0573-0165-251 in 1 CARTON 18/05/1984
736 in 1 BOTTLE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0154
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FERRIC OXIDE RED(UNII: 1K09F3G675)
METHYLPARABEN(UNII: A2I8C7HI9T)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
SHELLAC(UNII: 46N107B71O)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM BENZOATE(UNII: OJ245FE5EU)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WHITE WAX(UNII: 7G1J5DA97F)
DIACETYLATED MONOGLYCERIDES(UNII: 5Z17386USF)
Product Characteristics
Color brown (pinkish brown) Score no score
Shape ROUND Size 11 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0154-351 in 1 CARTON 18/05/1984
1150 in 1 BOTTLE Type 0: Not a Combination Product
2NDC:0573-0154-751 in 1 CARTON 18/05/1984
2200 in 1 BOTTLE Type 0: Not a Combination Product
3NDC:0573-0154-173000 in 1 CASE 18/05/1984
32 in 1 POUCH Type 0: Not a Combination Product
4NDC:0573-0154-8950 in 1 CASE 18/05/1984
42 in 1 POUCH Type 0: Not a Combination Product
5NDC:0573-0154-841 in 1 CARTON 18/05/1984
5225 in 1 BOTTLE Type 0: Not a Combination Product
6NDC:0573-0154-98300 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
7NDC:0573-0154-163 in 1 CARTON 18/05/1984
72 in 1 POUCH Type 0: Not a Combination Product18/05/1984
8NDC:0573-0154-60360 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
9NDC:0573-0154-591 in 1 CARTON 18/05/1984
9200 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
10NDC:0573-0154-21200 in 1 BOTTLE Type 0: Not a Combination Product01/04/2016
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0151
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FERRIC OXIDE RED(UNII: 1K09F3G675)
METHYLPARABEN(UNII: A2I8C7HI9T)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
SHELLAC(UNII: 46N107B71O)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM BENZOATE(UNII: OJ245FE5EU)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WHITE WAX(UNII: 7G1J5DA97F)
DIACETYLATED MONOGLYCERIDES(UNII: 5Z17386USF)
Product Characteristics
Color brown (pinkish brown) Score no score
Shape ROUND Size 11 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0151-1210 in 1 VIAL Type 0: Not a Combination Product18/05/1984
2NDC:0573-0151-133 in 1 PACKAGE 18/05/1984
210 in 1 VIAL Type 0: Not a Combination Product18/05/1984
3NDC:0573-0151-1010 in 1 PACKAGE 18/05/1984
310 in 1 VIAL Type 0: Not a Combination Product18/05/1984
4NDC:0573-0151-211 in 1 CARTON 18/05/1984
436 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
5NDC:0573-0151-202 in 1 PACKAGE 18/05/1984
510 in 1 VIAL Type 0: Not a Combination Product18/05/1984
6NDC:0573-0151-482 in 1 PACKAGE 18/05/1984
61 in 1 CARTON 18/05/1984
6100 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
7NDC:0573-0151-301 in 1 CARTON 18/05/1984
7130 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
8NDC:0573-0151-051 in 1 CARTON 18/05/1984
8115 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0161
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FERRIC OXIDE RED(UNII: 1K09F3G675)
METHYLPARABEN(UNII: A2I8C7HI9T)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
SHELLAC(UNII: 46N107B71O)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM BENZOATE(UNII: OJ245FE5EU)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WHITE WAX(UNII: 7G1J5DA97F)
DIACETYLATED MONOGLYCERIDES(UNII: 5Z17386USF)
Product Characteristics
Color brown (pinkish brown) Score no score
Shape OVAL Size 15 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0161-351 in 1 CARTON 18/05/1984
1150 in 1 BOTTLE Type 0: Not a Combination Product
2NDC:0573-0161-511 in 1 CARTON 18/05/1984
2200 in 1 BOTTLE Type 0: Not a Combination Product
3NDC:0573-0161-851 in 1 CARTON 18/05/1984
3225 in 1 BOTTLE Type 0: Not a Combination Product
4NDC:0573-0161-6565 in 1 BOTTLE Type 0: Not a Combination Product05/01/2017
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0166
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FD&C RED NO. 40(UNII: WZB9127XOA)
FD&C YELLOW NO. 6(UNII: H77VEI93A8)
FERRIC OXIDE RED(UNII: 1K09F3G675)
GELATIN, UNSPECIFIED(UNII: 2G86QN327L)
GLYCERIN(UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED(UNII: 3NXW29V3WO)
MEDIUM-CHAIN TRIGLYCERIDES(UNII: C9H2L21V7U)
PROPYL GALLATE(UNII: 8D4SNN7V92)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
TRIACETIN(UNII: XHX3C3X673)
WATER(UNII: 059QF0KO0R)
Product Characteristics
Color brown (one side is brown while the other side is yellow) Score no score
Shape OVAL Size 16 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0166-511 in 1 CARTON 18/05/1984
1200 in 1 BOTTLE Type 0: Not a Combination Product
2NDC:0573-0166-85225 in 1 BOTTLE Type 0: Not a Combination Product18/05/1984
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0150
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FERRIC OXIDE RED(UNII: 1K09F3G675)
METHYLPARABEN(UNII: A2I8C7HI9T)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
SHELLAC(UNII: 46N107B71O)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM BENZOATE(UNII: OJ245FE5EU)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WHITE WAX(UNII: 7G1J5DA97F)
DIACETYLATED MONOGLYCERIDES(UNII: 5Z17386USF)
Product Characteristics
Color brown (pinkish brown) Score no score
Shape ROUND Size 11 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0150-201 in 1 CARTON 18/05/1984
124 in 1 BOTTLE Type 0: Not a Combination Product
2NDC:0573-0150-301 in 1 CARTON 18/05/1984
250 in 1 BOTTLE Type 0: Not a Combination Product
3NDC:0573-0150-401 in 1 CARTON 18/05/1984
3100 in 1 BOTTLE Type 0: Not a Combination Product
4NDC:0573-0150-311 in 1 CARTON 18/05/1984
475 in 1 BOTTLE Type 0: Not a Combination Product
5NDC:0573-0150-321 in 1 CARTON 18/05/1984
560 in 1 BOTTLE Type 0: Not a Combination Product
6NDC:0573-0150-411 in 1 CARTON 18/05/1984
6125 in 1 BOTTLE Type 0: Not a Combination Product
7NDC:0573-0150-421 in 1 CARTON 18/05/1984
7150 in 1 BOTTLE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-0160
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FERRIC OXIDE RED(UNII: 1K09F3G675)
METHYLPARABEN(UNII: A2I8C7HI9T)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
SHELLAC(UNII: 46N107B71O)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM BENZOATE(UNII: OJ245FE5EU)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WHITE WAX(UNII: 7G1J5DA97F)
DIACETYLATED MONOGLYCERIDES(UNII: 5Z17386USF)
Product Characteristics
Color brown (pinkish brown) Score no score
Shape OVAL Size 15 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-0160-201 in 1 CARTON 18/05/1984
124 in 1 BOTTLE Type 0: Not a Combination Product
2NDC:0573-0160-301 in 1 CARTON 18/05/1984
250 in 1 BOTTLE Type 0: Not a Combination Product
3NDC:0573-0160-401 in 1 CARTON 18/05/1984
3100 in 1 BOTTLE Type 0: Not a Combination Product
4NDC:0573-0160-251 in 1 CARTON 18/05/1984
436 in 1 BOTTLE Type 0: Not a Combination Product
5NDC:0573-0160-311 in 1 CARTON 18/05/1984
575 in 1 BOTTLE Type 0: Not a Combination Product
6NDC:0573-0160-411 in 1 CARTON 18/05/1984
6125 in 1 BOTTLE Type 0: Not a Combination Product
7NDC:0573-0160-421 in 1 CARTON 18/05/1984
7150 in 1 BOTTLE Type 0: Not a Combination Product
8NDC:0573-0160-171 in 1 CARTON 18/05/1984
8115 in 1 BOTTLE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984
ADVILibuprofen TABLET, COATED
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-1711
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IBUPROFEN(UNII: WK2XYI10QM)
(IBUPROFEN - UNII:WK2XYI10QM) 		IBUPROFEN200 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE(UNII: OP1R32D61U)
CROSCARMELLOSE SODIUM(UNII: M28OL1HH48)
FERRIC OXIDE RED(UNII: 1K09F3G675)
METHYLPARABEN(UNII: A2I8C7HI9T)
POVIDONE, UNSPECIFIED(UNII: FZ989GH94E)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
SHELLAC(UNII: 46N107B71O)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM BENZOATE(UNII: OJ245FE5EU)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
STARCH, CORN(UNII: O8232NY3SJ)
STEARIC ACID(UNII: 4ELV7Z65AP)
SUCROSE(UNII: C151H8M554)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
WHITE WAX(UNII: 7G1J5DA97F)
DIACETYLATED MONOGLYCERIDES(UNII: 5Z17386USF)
Product Characteristics
Color brown (pinkish brown) Score no score
Shape ROUND Size 11 mm
Flavor Imprint Code Advil
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0573-1711-141 in 1 CARTON 18/05/1984
1225 in 1 BOTTLE Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA018989 05/18/1984

LABELER - Haleon US Holdings LLC(079944263)

PRINCIPAL DISPLAY PANEL

NDC 0573-0165-40

Advil

Ibuprofen Tablets, 200 mg
Pain Reliever / Fever Reducer (NSAID)

100 Coated Gel Caplets*
*Capsule-Shaped Gelatin-Coated Tablets

Gel
Caplets

000067202 Front Carton

Advil Gel Caps 100ct

PRINCIPAL DISPLAY PANEL

Advil ®
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

300 Coated Tablets

Tablets

Advil Coated Tablets 300ct

PRINCIPAL DISPLAY PANEL

15
FREE
TABLETS

Advil ®
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

115
Coated Tablets

Tablets

Advil Coated Tablets 115

PRINCIPAL DISPLAY PANEL

25
FREE
CAPLETS

Advil ®
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

225
Coated Caplets*
*Capsule-Shaped Tablets

Caplets

Advil Coated Caplets 225 ct

PRINCIPAL DISPLAY PANEL

NDC 0573-0150-20

Advil
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

24 Coated Tablets

Tablets

000067199 Front Carton

Advil Tablets 24ct

PRINCIPAL DISPLAY PANEL

Advil ®
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

100 Tablets

Tablets

READ AND KEEP CARTON FOR COMPLETE
WARNINGS AND INFORMATION

Do Not Use if seal under bottle cap imprinted with
"SEALED for YOUR PROTECTION" is broken or missing.

Advil Tablets 100ct

PRINCIPAL DISPLAY PANEL

NDC 0573-0160-20

Advil
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

24 Coated Caplets*
*Capsule-Shaped Tablets

Caplets

000067201 Front Carton

Advil Tablets Capsule Shaped 24ct

PRINCIPAL DISPLAY PANEL

NDC 0573-1711-14

Advil®
Ibuprofen Tablets, 200 mg
Pain Reliever/Fever Reducer (NSAID)

225 Caplets

Caplets

READ AND KEEP CARTON FOR COMPLETE
WARNINGS AND INFORMATION

PAA085439 Bottle Label

PAA085439 Advil Caplets 225 Caplets