DERMACLEAR BHA SPOT TREATMENT- salicylic acid gel

DermaClear BHA Spot Treatment by

Drug Labeling and Warnings

DermaClear BHA Spot Treatment 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 - 2%

PURPOSE

Purpose: Acne Treatment

INDICATIONS & USAGE

Uses:

• For the treatment of acne.

WARNINGS

Warnigs

• For external use only

WHEN USING

When using this product

• Avoid contact with eyes, lips and mouth.
• Using other topical acne medication at the same time ot immefiately 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.
• If sensitive to the sun or when increased sun exposure is expected use a sunscreen.

STOP USE

Stop use and ask a doctor:

• If severe skin irritation occurs.
• Using other topical medication at the same time

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

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

DOSAGE & ADMINISTRATION

Directions

• Apply a small portion over the affected area with finger tips and gently massage onto the skin.
• Reapply as needed.

INACTIVE INGREDIENT

Other ingredients:

Water (aqua), SD Alcohol 40-B, Butylene Glycol, Hydroxypropylcellulose

PRINCIPAL DISPLAY PANEL

Manufactured For Dermaquest ®, Inc.

Hayward, CA 94544

1272 GK, NL Made in USA

dermaquestinc.com

INGREDIENTS AND APPEARANCE

DERMACLEAR BHA SPOT TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62742-4195
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 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
ALCOHOL (UNII: 3K9958V90M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62742-4195-2	1 in 1 CARTON	12/10/2020
1	NDC: 62742-4195-1	4.8 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/10/2020

Labeler - Allure Labs (926831603)

Registrant - Allure Labs (926831603)

Establishment
Name	Address	ID/FEI	Business Operations
Allure Labs		926831603	manufacture(62742-4195)