NDC Code(s) : 10812-398-01
Packager : Johnson & Johnson Consumer Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Neutrogena All in 1 Acne Control Salicylic Acid LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10812-398
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Salicylic Acid(UNII: O414PZ4LPZ)
(Salicylic Acid - UNII:O414PZ4LPZ) 		Salicylic Acid20 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
Water(UNII: 059QF0KO0R)
Cetyl Alcohol(UNII: 936JST6JCN)
High Density Polyethylene(UNII: UG00KM4WR7)
Steareth-21(UNII: 53J3F32P58)
Polysorbate 60(UNII: CAL22UVI4M)
Potassium Cetyl Phosphate(UNII: 03KCY6P7UT)
Xanthan Gum(UNII: TTV12P4NEE)
Edetate Disodium(UNII: 7FLD91C86K)
Menthyl Lactate, (-)-(UNII: 2BF9E65L7I)
Sodium Hydroxide(UNII: 55X04QC32I)
Soybean(UNII: L7HT8F1ZOD)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:10812-398-01125 mL in 1 TUBE Type 0: Not a Combination Product30/11/2011
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333D 11/30/2011 06/01/2018

PRINCIPAL DISPLAY PANEL

NEW INFO

All-in-1
Acne
Control
daily scrub

clears up acne's
past, present & future

  • fades the look of past acne marks
  • clears present breakouts
  • helps prevent future breakouts

Neutrogena®

salicylic acid acne treatment

4.2 FL. OZ. (125mL)

Principal Display Panel - 125 mL Tube Label