NDC | 49967-875-01, 49967-875-02, 49967-875-03 |
Set ID | 3346f5f8-5793-47f6-8e71-250d3cc05c0d |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333D |
- Active ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Keep out of reach of children.
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
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Inactive ingredients
water, aloe barbadensis leaf juice, di-C12-13 alkyl malate, niacinamide, cyclohexasiloxane, propylene glycol, aluminum starch octenylsuccinate, PEG-100 stearate, glyceryl stearate, cetyl alcohol, acrylates/C10-30 alkyl acrylate crosspolymer, sodium hydroxide, capryloyl salicylic acid, xanthan gum, zinc PCA, zingiber officinale (ginger) root extract, stearyl alcohol, myristyl alcohol, citric acid, potassium sorbate, octadecenedioic acid, sodium benzoate, citral, BHT
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS BREAKOUT CONTROL ACNE TREATMENT FACIAL
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-875 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) NIACINAMIDE (UNII: 25X51I8RD4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294) PEG-100 STEARATE (UNII: YD01N1999R) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM HYDROXIDE (UNII: 55X04QC32I) CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) XANTHAN GUM (UNII: TTV12P4NEE) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) MYRISTYL ALCOHOL (UNII: V42034O9PU) OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG) CITRAL (UNII: T7EU0O9VPP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-875-01 1 in 1 CARTON 11/01/2016 1 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-875-02 5 mL in 1 PACKET; Type 0: Not a Combination Product 11/01/2016 3 NDC:49967-875-03 1.5 mL in 1 PACKET; Type 0: Not a Combination Product 11/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 11/01/2016 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-875)