Label: OXY MAXIMUM STRENGTH RAPID SPOT TREATMENT cream
- NDC Code(s): 10742-1002-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 5, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
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 use a sunscreen
- avoid contact 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 1 to 3 times daily
- once dry, follow with a non-comedogenic moisturizer if needed
- because excessive drying of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or 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.
- Other information
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Inactive ingredients
water, glycerin, butylene glycol, carbomer, chlorphenesin, citric acid, dimethyl isosorbide, disodium EDTA, fragrance, hydrated silica, hydrolyzed soy protein, lauryl methacrylate/glycol dimethacrylate crosspolymer, PEG/PPG-4/12 dimethicone, phenoxyethanol, portulaca oleracea extract, propanediol, rhodomyrtus tomentosa fruit extract, sodium citrate, sodium hydroxide, xanthan gum
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INGREDIENTS AND APPEARANCE
OXY MAXIMUM STRENGTH RAPID SPOT TREATMENT
oxy maximum strength rapid spot treatment creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1002 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 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CITRIC ACID (UNII: 2968PHW8QP) HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6) PEG/PPG-4/12 DIMETHICONE (UNII: JAN3585W85) PROPANEDIOL (UNII: 5965N8W85T) SODIUM HYDROXIDE (UNII: 55X04QC32I) PORTULACA OLERACEA LEAF (UNII: 9JW9D9JGHZ) RHODOMYRTUS TOMENTOSA FRUIT (UNII: Q99511S58K) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER (UNII: 0A5MM307FC) HYDRATED SILICA (UNII: Y6O7T4G8P9) PHENOXYETHANOL (UNII: HIE492ZZ3T) FRAGRANCE 13576 (UNII: 5EM498GW35) SODIUM CITRATE (UNII: 1Q73Q2JULR) XANTHAN GUM (UNII: TTV12P4NEE) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CHLORPHENESIN (UNII: I670DAL4SZ) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1002-1 1 in 1 CARTON 08/15/2024 1 28 g 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 08/15/2024 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-1002)
