NDC | 49967-617-01, 49967-617-02, 49967-617-03 |
Set ID | effa0d12-65b5-48b7-a4eb-9177f58b2539 |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333D |
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
-
Inactive ingredients
water, coco-glucoside, propylene glycol, sorbitol, sodium laureth sulfate, treithanolamine, sodium chloride, PEG-120 methyl glucose dioleate, menthol, methylparaben, imidazolidinyl urea, benzophenone-4, disodium EDTA, dipropylene glycol, camphor, zinc PCA, aloe barbadensis leaf juice, boswella serrata extract, laminaria saccharina extract, blue 1, poterium officinale root extract, zinber officinale (ginger) root extract, cinnamomum cassia bark extract, hammamelis virginiana (witch hazel) leaf extract
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 BLUE HERBAL GEL CLEANSER ACNE TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-617 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) COCO-BETAINE (UNII: 03DH2IZ3FY) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SORBITOL (UNII: 506T60A25R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM CHLORIDE (UNII: 451W47IQ8X) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) MENTHOL (UNII: L7T10EIP3A) METHYLPARABEN (UNII: A2I8C7HI9T) DIPROPYLENE GLYCOL (UNII: E107L85C40) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) WITCH HAZEL (UNII: 101I4J0U34) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-617-01 125 mL in 1 TUBE; Type 0: Not a Combination Product 02/03/2014 2 NDC:49967-617-02 200 mL in 1 TUBE; Type 0: Not a Combination Product 02/03/2014 3 NDC:49967-617-03 250 mL in 1 TUBE; Type 0: Not a Combination Product 02/03/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 02/03/2014 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-617)