BHA TONER- salicylic acid spray

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Use

For the treatment of acne

Warnings

For external use only.

When using this product Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. Avoid contact with eyes, lips and mouth. If contact occurs, flush thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Spray toner directly on face or on cotton pad. Apply to face and neck, avoiding the eye area. Repeat until minimal dirt is visible. Can be used twice daily or as directed by a physician.

Inactive ingredients

Water/Aqua/Eau, Glycerin, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Menthyl Lactate, Allantoin, Panthenol, Papaya (Carica Papaya) Fruit Extract, Olive (Olea Europaea) Leaf Extract, Rosemary (Rosmarinus Officinalis) Leaf Extract, Benzophenone-4, Sodium PCA, Fragrance (Parfum), Beta-Glucan, Limonene, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090)

Questions or comments?

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SPL UNCLASSIFIED SECTION

Unclog pores and prevent breakouts with salicylic acid 2%

Made in U.S.A. with globally sourced materials
Dist. by DRMTLGY LLC
Los Angeles, CA 91304
DRMTLGY.com

Packaging

INGREDIENTS AND APPEARANCE

BHA TONER 
salicylic acid spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83286-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
ALLANTOIN (UNII: 344S277G0Z)
PANTHENOL (UNII: WV9CM0O67Z)
PAPAYA (UNII: KU94FIY6JB)
OLEA EUROPAEA (OLIVE) LEAF POWDER (UNII: MJ95C3OH47)
ROSEMARY (UNII: IJ67X351P9)
SULISOBENZONE (UNII: 1W6L629B4K)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
OAT (UNII: Z6J799EAJK)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83286-018-01	189 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	05/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	05/01/2026

Labeler - Drmtlgy, LLC (094762235)