NDC Code(s) : 0363-8202-22, 0363-8202-29
Packager : Walgreens

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Walgreens Fluoride PASTE, DENTIFRICE
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0363-8202
Route of Administration DENTAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM FLUORIDE(UNII: 8ZYQ1474W7)
(FLUORIDE ION - UNII:Q80VPU408O) 		FLUORIDE ION0.243 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
SACCHARIN SODIUM(UNII: SB8ZUX40TY)
SORBITOL(UNII: 506T60A25R)
TITANIUM DIOXIDE(UNII: 15FIX9V2JP)
SODIUM HYDROXIDE(UNII: 55X04QC32I)
XANTHAN GUM(UNII: TTV12P4NEE)
HYDRATED SILICA(UNII: Y6O7T4G8P9)
SODIUM ACID PYROPHOSPHATE(UNII: H5WVD9LZUD)
CARBOXYMETHYLCELLULOSE SODIUM(UNII: K679OBS311)
CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)(UNII: HHT01ZNK31)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
MICA(UNII: V8A1AW0880)
Product Characteristics
Color blue Score
Shape Size
Flavor MINT Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:0363-8202-291 in 1 CARTON
1NDC:0363-8202-22113 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part356 01/20/2011

PRINCIPAL DISPLAY PANEL

mm1.jpg

Carton label

mm2.jpg

Carton label