NDC | 49967-616-01, 49967-616-02 |
Set ID | 8e1e86ca-c567-465b-9993-ddb5f97bb5f5 |
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, glycerin, montmorillonie, dimethicone, cyclohexasiloxane, glyceryl stearate SE, polyglyceryl-3 methylglycose distearate, stearyl alcohol, pentylene glycol, propylene glycol, methylparaben, chlorphenesin, xanthan gum, carbomer, sodium hydroxide, sodium PCA, butylparaben, dipropylene glycol, tetrasodium EDTA, laminaria saccharina extract, menthol, aloe barbadensis leaf juice, bosewella serrata extract, camphor, hammamelis virginiana (witch hazel) leaf extract, poterium officinale root extract, zinglber officinale (ginger) root extrct, cinnamomum cassia bark extract, blue 1
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 BLUE HERBAL MOISTURIZER ACNE TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-616 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CHLORPHENESIN (UNII: I670DAL4SZ) XANTHAN GUM (UNII: TTV12P4NEE) CARBOMER HOMOPOLYMER TYPE B (ALLYL PENTAERYTHRITOL OR ALLYL SUCROSE CROSSLINKED) (UNII: K6MOM3T5YL) SODIUM HYDROXIDE (UNII: 55X04QC32I) BUTYLPARABEN (UNII: 3QPI1U3FV8) DIPROPYLENE GLYCOL (UNII: E107L85C40) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) CAMPHOR (NATURAL) (UNII: N20HL7Q941) WITCH HAZEL (UNII: 101I4J0U34) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-616-01 100 mL in 1 TUBE; Type 0: Not a Combination Product 02/03/2014 2 NDC:49967-616-02 3 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(49967-616)