HUMANE ACNE WASH- benzoyl peroxide liquid 
Apprendista, LLC

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HUMANE ACNE WASH

Drug Facts

Active ingredient

Benzoyl Peroxide 10%

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 two to three times 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.

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 3-5 minutes for wash to absorb. Rinse thoroughly.

Inactive ingredients

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

Package Labeling:

Label

HUMANE ACNE WASH 
benzoyl peroxide liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73010-900
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73010-900-00237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00604/01/2019
Labeler - Apprendista, LLC (116995922)

Revised: 11/2023
Document Id: 097502bf-7222-dd2b-e063-6394a90a7520
Set id: 1d25fb25-a3d2-4c6b-a975-be7b90b70265
Version: 3
Effective Time: 20231105
 
Apprendista, LLC