- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
-
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.
- rinse right away with water if it gets in eyes
- 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
- Stop use adn ask a doctor if
- Keep out of reach of children.
-
Directions
- cleanse the skin thoroughly before applying medication
- cover the entire affected area with a thin layer one to three times a day
- because excessive drying og 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 or every other day.
- if going outside, use a sunscreen. Allow product to dry, then follow direction in the sunscreen labeling. If sensitivity develops, discontinue use of both products and consult a doctor.
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
VANISHING ACNE CVS
10% benzoyl peroxide acne medication creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-048 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 10 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLUCONOLACTONE (UNII: WQ29KQ9POT) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERIN (UNII: PDC6A3C0OX) PEG-40 STEARATE (UNII: ECU18C66Q7) CETYL ALCOHOL (UNII: 936JST6JCN) DIMETHICONE (UNII: 92RU3N3Y1O) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) AMMONIA (UNII: 5138Q19F1X) ISOPROPYLPARABEN (UNII: A6EOX47QK0) BUTYLPARABEN (UNII: 3QPI1U3FV8) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) ARGININE (UNII: 94ZLA3W45F) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-048-01 1 in 1 CARTON 12/13/2013 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 final part333D 12/13/2013 Labeler - CVS (062312574) Registrant - Product Quest Mff, LLC (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mff, LLC 927768135 manufacture(69842-048)