HUMANE ACNE SPOT TREATMENT- benzoyl peroxide gel 
Apprendista, LLC

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HUMANE Acne Spot Treatment Gel

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 
  • have very sensitive skin.

When using this product

  • Skin irritation and dryness are 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 unnecessary sun exposure and use a sunscreen. 
  • Avoid contact with eyes, lips and mouth. Avoid product contact with hair and dyed fabrics, which may be bleached by this product.
  • Skin irritation may occur, characterized by redness, burning, itching, peeling, or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

Stop use and ask a doctor

if irritation becomes severe.

Keep out of reach of children:

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

If pregnant or breast-feeding,

ask a health professional before use.

Directions

Inactive ingredients

a-Bisabalol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Caprylyl Glycol, Cucumis Sativus (Cucumber) Extract, Glycyrrhiza Glabra (Licorice) Extract, Hexylene Glycol, Menthyl Lactate, Phenoxyethanol, Polysorbate-20, Potassium Sorbate, Propylene Glycol, Sodium Hydroxide

Questions?

thehumanecompany.com

Package Labeling:

Label

HUMANE ACNE SPOT TREATMENT 
benzoyl peroxide gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73010-127
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
ALLANTOIN (UNII: 344S277G0Z)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CUCUMBER (UNII: YY7C30VXJT)  
LICORICE (UNII: 61ZBX54883)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73010-127-001 in 1 BOX03/01/2021
130 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00603/01/2021
Labeler - Apprendista, LLC (116995922)

Revised: 11/2023
Document Id: 09dc7f08-9210-435a-e063-6394a90a8dca
Set id: ceeb398e-c516-45e4-a21c-cbecf6206fcc
Version: 3
Effective Time: 20231111
 
Apprendista, LLC