TEXTURE ID ANTI DANDRUFF OIL TREATMENT- salicylic acid oil

Texture ID Anti Dandruff Oil Treatment by

Drug Labeling and Warnings

Texture ID Anti Dandruff Oil Treatment 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 OIL TREATMENT 
salicylic acid oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60717-412
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
SOYBEAN OIL (UNII: 241ATL177A)
FRAGRANCE 13576 (UNII: 5EM498GW35)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)
MENTHA PIPERITA (PEPPERMINT) OIL (UNII: AV092KU4JH)
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393)
MENTHOL (UNII: L7T10EIP3A)
TERPINEOL (UNII: R53Q4ZWC99)
CITRONELLOL (UNII: P01OUT964K)
PRUNUS AMYGDALUS DULCIS (SWEET ALMOND) OIL (UNII: 66YXD4DKO9)
RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G)
GERANIOL (UNII: L837108USY)
CITRUS AURANTIUM PEEL OIL (UNII: 9TLV70SV6I)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
HEXYL CINNAMAL (UNII: 7X6O37OK2I)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
ISOPROPYL LAURATE (UNII: U0JQ94LABM)
CARVONE, (+)- (UNII: 4RWC1CMS3X)
TETRAMETHYL ACETYLOCTAHYDRONAPHTHALENES (UNII: 2JU6ZH6GRE)
BETA-CARYOPHYLLENE (UNII: BHW853AU9H)
PINENE (UNII: 996299PUKB)
TOCOPHEROL (UNII: R0ZB2556P8)
MENTHA VIRIDIS (SPEARMINT) LEAF OIL (UNII: C3M81465G5)
LINALOOL (UNII: D81QY6I88E)
LINALYL ACETATE (UNII: 5K47SSQ51G)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CITRUS AURANTIUM BERGAMIA (BERGAMOT) PEEL OIL (UNII: 39W1PKE3JI)

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60717-412-04	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(60717-412)