Label: TERMINATOR 10- benzoyl peroxide cream
- NDC Code(s): 80861-002-01
- Packager: AcneFree, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 19, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Use
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Warnings
For external use only
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.
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Directions
- clean the skin thoroughly before applying this product
- cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day every other day
- if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor
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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
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INGREDIENTS AND APPEARANCE
TERMINATOR 10
benzoyl peroxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80861-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:80861-002-01 1 in 1 CARTON 12/26/2017 1 30 mL in 1 TUBE; 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 12/26/2017 Labeler - AcneFree, LLC (122237140)
