NDC | 49967-615-01, 49967-615-02 |
Set ID | 344bedc1-5228-4543-898e-895cac0bc336 |
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.
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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 ingrease to two or three times dialy if neded or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl
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Inactive ingredients
water, alcohol denat., glycerin, glycolic acid, triethanolamine, ammonium polyacryloyldimethyl taurate, acrylates/C10-30 alkyl acrylate crosspolymer, pentylene glycol, butylene glycol, zinc gluconate, propylelne glycol, dipropylene glycol, camphor, menthol, aloe barbadensis leaf juice, boswellia serrata extract, laminaria saccharina extract, hammamelis viginiana (witch hazel) leaf extract, potarium officinale root exract, zingiber officinale (ginger) root extract, cimmamoum casaia bark extract
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 BLUE HERBAL SPOT TREATMENT ACNE
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-615 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) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) GLYCOLIC ACID (UNII: 0WT12SX38S) TROLAMINE (UNII: 9O3K93S3TK) PENTYLENE GLYCOL (UNII: 50C1307PZG) DIPROPYLENE GLYCOL (UNII: E107L85C40) CAMPHOR (NATURAL) (UNII: N20HL7Q941) MENTHOL (UNII: L7T10EIP3A) WITCH HAZEL (UNII: 101I4J0U34) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-615-01 1 in 1 CARTON 02/03/2014 1 15 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-615-02 1.5 mL in 1 PACKET; 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(49967-615)