Label: TEXTURE ID ANTI DANDRUFF PEPPERMINT OIL AND ALOE- salicylic acid lotion/shampoo
- NDC Code(s): 60717-410-12
- Packager: RNA PHARMA, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 2, 2025
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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INGREDIENTS AND APPEARANCE
TEXTURE ID ANTI DANDRUFF PEPPERMINT OIL AND ALOE
salicylic acid lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60717-410 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.02 g in 1 g Inactive Ingredients Ingredient Name Strength PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) PHENOXYETHANOL (UNII: HIE492ZZ3T) MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM BENZOATE (UNII: OJ245FE5EU) POLYQUATERNIUM-10 (1400 MPA.S AT 2%) (UNII: W6F63XD4Z3) WATER (UNII: 059QF0KO0R) AMINOMETHYL PROPANOL (UNII: LU49E6626Q) BENZOIC ACID (UNII: 8SKN0B0MIM) COCO-GLUCOSIDE (UNII: ICS790225B) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ISOPROPYL ALCOHOL (UNII: ND2M416302) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) EDETATE DISODIUM (UNII: 7FLD91C86K) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) BETAINE (UNII: 3SCV180C9W) PEPPERMINT OIL (UNII: AV092KU4JH) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) CITRIC ACID (UNII: 2968PHW8QP) GLYCERETH-2 COCOATE (UNII: JWM00VS7HC) HYDROXYPROPYL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: MVW5LK6LFT) POLYQUATERNIUM-7 (UNII: 0L414VCS5Y) ALMOND OIL (UNII: 66YXD4DKO9) SODIUM HYDROXIDE (UNII: 55X04QC32I) SODIUM ACETATE (UNII: 4550K0SC9B) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) Product Characteristics Color white (Translucent Colorless) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60717-410-12 1 g in 1 BOTTLE; Type 0: Not a Combination Product 09/25/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M014 09/25/2025 Labeler - RNA PHARMA, LLC (079103999) Establishment Name Address ID/FEI Business Operations RNA PHARMA, LLC 079103999 manufacture(60717-410)
