TERMINATOR 10- benzoyl peroxide cream 
AcneFree, LLC

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Terminator 10

Drug Facts

Active ingredient

Benzoyl peroxide 10%

Purpose

Acne treatment

Use

for the treatment of acne

Warnings

For external use only

Do not use on if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product

  • skin irritation and dryness is 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 a sunscreen
  • avoid contat with the eyes, lips, and mouth
  • avoid 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

skin irritation becomes severe

Keep out of reach of children.

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

Directions

Inactive ingredients

acrylates/C10-30 alkyl crosspolymer, benzalkonium chloride, bisabolol, butylene glycol, chamomilla recutita (matricaria) flower extract, ethylhexylglycerin, glycerin, methyl methacrylate/glycol dimethacrylate crosspolymer, methylpropanediol, phenoxyethanol, sea whip extract, sodium benzoate, sodium hydroxide, tetrasodium EDTA, water, zingiber officinale (ginger) root extract

Questions or comments?

1-888-768-2913

Package Labeling:

carton2Tube2

TERMINATOR 10 
benzoyl peroxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80861-002
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
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
LEVOMENOL (UNII: 24WE03BX2T)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CHAMOMILE (UNII: FGL3685T2X)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
GINGER (UNII: C5529G5JPQ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80861-002-011 in 1 CARTON12/26/2017
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 DrugM00612/26/2017
Labeler - AcneFree, LLC (122237140)

Revised: 6/2024
Document Id: 1b3f725e-9aec-aed0-e063-6394a90af41c
Set id: c06778b6-0ed6-7d82-e053-2a95a90a2ef8
Version: 5
Effective Time: 20240619
 
AcneFree, LLC