NDC Code(s) : 45802-939-02
Packager : Perrigo New York Inc

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Seb Prev Sodium Sulfacetamide LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:45802-939
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 0.95 mL
Inactive Ingredients
Ingredient Name Strength
EDETATE DISODIUM(UNII: 7FLD91C86K)
METHYLPARABEN(UNII: A2I8C7HI9T)
WATER(UNII: 059QF0KO0R)
SODIUM LAURETH-3 SULFATE(UNII: BPV390UAP0)
SODIUM THIOSULFATE(UNII: HX1032V43M)
COCAMIDOPROPYL BETAINE(UNII: 5OCF3O11KX)
PEG-6 CAPRYLIC/CAPRIC GLYCERIDES(UNII: GO50W2HWO8)
PEG-60 ALMOND GLYCERIDES(UNII: 4Y0E651N0F)
PEG-150 PENTAERYTHRITYL TETRASTEARATE(UNII: 8L4OOQ76AM)
Product Characteristics
Color WHITE (off-white) Score
Shape Size
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:45802-939-02340 mL in 1 BOTTLE Type 0: Not a Combination Product28/07/2008
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
Unapproved drug other 07/25/2008 09/30/2018

PRINCIPAL DISPLAY PANEL

Rx Only

SEB-Prev™ Wash

(Sodium Sulfacetamide 10%)

WARNING: For Dermatological Use Only. Not for Ophthalmic or Intravaginal Use.

SEB-Prev (TM) Wash Sodium Sulfacetamide 10%) Label Image