KERASTASE PARIS K SYMBIOSE SERUM NUIT ANTIPELLICULAIRE INTENSIF ANTIDANDRUFF TREATMENT- salicylic acid liquid

Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment by

Drug Labeling and Warnings

Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc., Interspray. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 1.8%

Purpose

Antidandruff

Use

• helps eliminate the symptoms of dandruff

Warnings

For external use only

When using this product

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

condition worsens or does not improve after regular use of this product as directed

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply to affected areas one to 4 times daily or as directed by a doctor 
• use before going to bed for 4 weeks
• apply 4 doses on scalp section by section (1 dose = 1 pipette)
• do not rinse

Inactive ingredients

water, alcohol denat., aminomethyl propanol, fragrance, PEG-40 hydrogenated castor oil, bifida ferment lysate, limonene, glycerin, benzyl salicylate, benzyl alcohol, linalool, citronellol, citral, geraniol, artemisia umbelliformis flower extract, coumarin, phenoxyethanol, sodium benzoate, citric acid, potassium sorbate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KERASTASE PARIS K SYMBIOSE SERUM NUIT ANTIPELLICULAIRE INTENSIF ANTIDANDRUFF TREATMENT 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-363
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	18 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
GLYCERIN (UNII: PDC6A3C0OX)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
BENZYL ALCOHOL (UNII: LKG8494WBH)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
CITRAL (UNII: T7EU0O9VPP)
GERANIOL (UNII: L837108USY)
ARTEMISIA UMBELLIFORMIS FLOWER (UNII: 91OLL9AJ7D)
COUMARIN (UNII: A4VZ22K1WT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-363-01	1 in 1 CARTON	12/01/2022
1		90 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	12/01/2022

Labeler - L'Oreal USA Products Inc. (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
Interspray		364829903	manufacture(49967-363)