- Active ingredient Purpose
- PURPOSE
- INDICATIONS & USAGE
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WarningsFor 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. • rinse right away with water if it gets in eyes • avoid unnecessary sun exposure and use a sunscreen •avoid contact with eyes, lips, and mouth • avoid contact with hair and dyed fabrics, which may be bleached by this product • skin irritation may occurs, 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
• cleans the skin thoroughly before applying medication • cover the entire affected area with a thin layer one to three times a day • 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 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 SAFETY INFORMATION
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VANISHING ACNE TREATMENT DAYLOGIC
benzoyl peroxide 10% creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-1229 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 Aluminum Hydroxide (UNII: 5QB0T2IUN0) Bentonite (UNII: A3N5ZCN45C) CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E) Glyceryl Stearate SE (UNII: FCZ5MH785I) Isopropyl Myristate (UNII: 0RE8K4LNJS) Methylparaben (UNII: A2I8C7HI9T) POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9) Potassium Hydroxide (UNII: WZH3C48M4T) Propylene Glycol (UNII: 6DC9Q167V3) Propylparaben (UNII: Z8IX2SC1OH) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-1229-1 1 in 1 CARTON 10/10/2011 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 10/10/2011 Labeler - Rite Aid (014578892) Registrant - Product Quest Mfg (927768135) Establishment Name Address ID/FEI Business Operations Product Quest Mfg 927768135 manufacture(11822-1229) , label(11822-1229)