CLEAR CHOICE BP 8 TOPICAL ACNE- benzoyl peroxide gel

Clear Choice BP 8 Topical Acne by

Drug Labeling and Warnings

Clear Choice BP 8 Topical Acne by is a Otc medication manufactured, distributed, or labeled by Dermastart Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRUG FACTS:

Active Ingredients

Benzoyl Peroxide 8%

Purpose

Acne Treatment

Indications:

• For the use of Acne
• Prevents future Acne breakouts
• Eliminates P-bacteria

Warnings:

For external use only - DO NOT APPLY TO BROKEN SKIN

- When using this product,

keep out of eyes. Rinse with water to remove. May bleach colored fabrics. Discontinue use if signs of rash or irritation appear.

Keep out of reach of children.

Keep this and all drugs out of reach of children in case of accidental ingestion, contact a Poison Control Center or get medical help.

Directions:

Apply over entire face or affected area. Dryness may occur, start with one daily application and increase as needed or as directed by your skincare professional. Avoid eye contact. Sunblock is recommended.

Inactive Ingredients:

Purified Water, Certified Organic Aloe Vera Gel, Japanese Green Tea Extract, Vegetable Glycerin, Cetearyl Alcohol (and) Ceteareth-20, Benzoyl Peroxide, Caprylic/Capric Triglycerides, Thiotic (Alpha Lipoic) Acid, Cetyl Alcohol, Dexapanthenol (Vitamin B5), Vitamin E Acetate, Lecithin, Retinyl Palmitate (Vitamin A), Sodium Hyaluronate, NaPCA, Extracts of Corn Silk, Alpha Bisabolol (Chamomile), Comfrey Root and Centella Asiatica, Magnesium Ascorbyl Phosphate (Vitamin C), and Grapeseed Extract.

Questions or comments?

Call toll free 1.866.589.2949

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Label

INGREDIENTS AND APPEARANCE

CLEAR CHOICE BP 8 TOPICAL ACNE 
benzoyl peroxide gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83722-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	80 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETYL ALCOHOL (UNII: 936JST6JCN)
PANTOTHENIC ACID (UNII: 19F5HK2737)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A (UNII: 81G40H8B0T)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CHAMOMILE (UNII: FGL3685T2X)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
VITIS VINIFERA SEED (UNII: C34U15ICXA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83722-001-00	60 mL in 1 TUBE; Type 0: Not a Combination Product	02/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	OKM006	02/07/2024

Labeler - Dermastart Inc (146909283)