NDC Code(s) : 42792-106-12
Packager : Austin Pharmaceuticals, LLC

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

SODIUM SULFACETAMIDESULFACETAMIDE SODIUM LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:42792-106
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SULFACETAMIDE SODIUM(UNII: 4NRT660KJQ)
(SULFACETAMIDE - UNII:4965G3J0F5) 		SULFACETAMIDE SODIUM100 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
COCAMIDOPROPYL BETAINE(UNII: 5OCF3O11KX)
EDETATE DISODIUM(UNII: 7FLD91C86K)
METHYLPARABEN(UNII: A2I8C7HI9T)
PEG-60 ALMOND GLYCERIDES(UNII: 4Y0E651N0F)
PEG-150 PENTAERYTHRITYL TETRASTEARATE(UNII: 8L4OOQ76AM)
PEG-6 CAPRYLIC/CAPRIC GLYCERIDES(UNII: GO50W2HWO8)
WATER(UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE(UNII: BPV390UAP0)
SODIUM THIOSULFATE(UNII: HX1032V43M)
Product Characteristics
Color yellow (light yellow) Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:42792-106-12355 mL in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product15/09/2011
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 09/15/2011 11/30/2015

PRINCIPAL DISPLAY PANEL

/xml/0f27adb1-cdb7-4ff1-a3c6-d395675b5858/label.jpg