HUMANE ACNE WASH 5- benzoyl peroxide liquid

HUMANE Acne Wash 5 by

Drug Labeling and Warnings

HUMANE Acne Wash 5 by is a Otc medication manufactured, distributed, or labeled by Banner 1 LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzoyl Peroxide 5%

Purpose

Acne Treatment

Use

for the treatment of acne.

Warnings

For external use only.

Do not use

• If you are sensitive to benzoyl peroxide or have very sensitive skin.
• Using other topical acne drugs at the same time or right after use of this product may increase dryness, redness or irritation of the skin.
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to twice daily if needed. If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

When using this product

• Avoid contact with and near eyes. If contact occurs, flush thoroughly with water. Keep away from lips and mouth.
• Avoid unnecessary sun exposure and use a sunscreen.
• Avoid product contact with hair and dyed fabrics, including carpets and clothing which may be bleached by this product.

Stop use and ask a doctor

if excessive irritation occurs.

Keep out of reach of children:

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

If pregnant or breastfeeding,

ask a health professional before use.

Directions

New User: Test 1-2 small affected areas for sensitivity for 3 days. If no discomfort occurs, apply acne wash and gently massage into damp skin. Wait 1-3 minutes for wash to absorb. Rinse thoroughly.

Inactive ingredients

Aqua (Deionized Water), Carbomer, Cocamidopropyl Betaine, Gluconolactone, Sodium Benzoate, Sodium Hydroxide

Questions?

thehumanecompany.com

69919-526-08

69919-526-16

INGREDIENTS AND APPEARANCE

HUMANE ACNE WASH 5 
benzoyl peroxide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69919-526
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69919-526-08	1 in 1 BOX	08/05/2024
1		237 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 69919-526-16	1 in 1 BOX	08/05/2024
2		473 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	M006	08/05/2024

Labeler - Banner 1 LLC (118714796)