Label: SHEA MOISTURE- apple cider vinegar anti-dandruff leave-in liquid
- NDC Code(s): 64942-2085-1
- Packager: Conopco, Inc. d/b/a/ Unilever
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 10, 2022
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- SHEA MOISTURE APPLE CIDER VINEGAR ANTI-DANDRUFF LEAVE-IN - salicylic acid liquid
- Drug Facts
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
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INGREDIENTS AND APPEARANCE
SHEA MOISTURE
apple cider vinegar anti-dandruff leave-in liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-2085 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.8 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM BENZOATE (UNII: OJ245FE5EU) MENTHOL (UNII: L7T10EIP3A) SHEA BUTTER (UNII: K49155WL9Y) WATER (UNII: 059QF0KO0R) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) SODIUM HYDROXIDE (UNII: 55X04QC32I) ACETIC ACID (UNII: Q40Q9N063P) GLYCERIN (UNII: PDC6A3C0OX) NIACINAMIDE (UNII: 25X51I8RD4) GLUCONOLACTONE (UNII: WQ29KQ9POT) ROSEMARY (UNII: IJ67X351P9) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-2085-1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 12/01/2022 Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)