TEXTURE ID ANTI DANDRUFF PEPPERMINT OIL AND ALOE- salicylic acid lotion/shampoo

Texture ID Anti Dandruff Peppermint Oil and Aloe by

Drug Labeling and Warnings

Texture ID Anti Dandruff Peppermint Oil and Aloe by is a Otc medication manufactured, distributed, or labeled by RNA PHARMA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

INACTIVE INGREDIENT

PURPOSE

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

WARNINGS

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TEXTURE ID ANTI DANDRUFF PEPPERMINT OIL AND ALOE 
salicylic acid lotion/shampoo

Product 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)