CLARIFYING TONER- salicylic acid liquid

Clarifying Toner by

Drug Labeling and Warnings

Clarifying Toner by is a Otc medication manufactured, distributed, or labeled by Allure Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient:

Salicylic Acid 1%

PURPOSE

Purpose: Acne Treatment

INDICATIONS & USAGE

Uses: For the treatment of acne

Gently cleanses and maintains optimal moisture balance.

For all skin types

WARNINGS

Warning: For external use only

DO NOT USE

If excessive dryness or peeling occurs.

WHEN USING

Avoid eye area.

STOP USE

If excessive dryness or peeling occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Direction:

Cleanse the skin thoroughly before applying medication. Avoid eye area. If excessive dryness or peeling occurs, reduce application to once a day.

OTHER SAFETY INFORMATION

Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation of the skin.If this occurs, only one medication should be used unless directed by a doctor.

INACTIVE INGREDIENT

Inactive Ingredient:

Water (Aqua), Alcohol Denat, Hamamelis Virginiana (Witch Hazel) Leaf Water, Ethoxydiglycol, Niacinamide, Glycerin, Polysorbate 20, Plantago Ovata (Indian Plantin) Seed Extract, Sodium PCA, Hydrolyzed Wheat Protein, Hydrolyzed Wheat Starch, Phenoxyethanol, Caprylyl Glycol, Ethylhexyl Glycerin, Rosmarinus Officinalis ( Rosemary) Leaf Extract, Chamomilla Recutita ( Chamomile) Flower Extract, Hexylene Glycol, Allantoin, Dipotassium Glycyrrhizate.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CLARIFYING TONER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4240
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 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ROSEMARY (UNII: IJ67X351P9)
MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02)
ALLANTOIN (UNII: 344S277G0Z)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PLANTAGO OVATA SEED (UNII: UD50RBY30F)
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
STARCH, WHEAT (UNII: 79QS2MG2LP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
WATER (UNII: 059QF0KO0R)
HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
NIACINAMIDE (UNII: 25X51I8RD4)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4240-1	120 g in 1 BOTTLE; Type 0: Not a Combination Product	12/08/2023
2	NDC: 62742-4240-2	60 g in 1 BOTTLE; Type 0: Not a Combination Product	12/08/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/08/2023

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4240)