- ACTIVE INGREDIENT
- PURPOSE
- Uses
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Warnings
For external use only.
DO NOT USE this product if you have sensitive skin or if you are sensitive to benzoyl peroxide
When using this product
Avoid unnecessary sun exposure and use sunscreen. Allow ZAPZYT acne gel to dry, then follow the sunscreen directions.
Avoid contact with hair or dyed fabric, including carpet and clothing which may be bleached by this product.
Skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. Mild irritation may be reduced by using this product less frequently or in a lower concentration. If irritation becomes severe, discontinue use; if irritation still occurs consult a doctor.
Using other topical acne medications at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
Keep away from eyes, lips and mouth
- OTC - Keep out of Reach of Children
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Directions
Use a ZAPZYT cleaning product to thoroughly wash face before applying gel.
Apply ZAPZYT Acne Treatment Gel to areas where pimples and excess oil occur
Apply ZAPZYT before using moisturizer or makeup; do not rinse.
If excessive drying of the skin occurs, reduce applications to once a day, or every other day.
For best results use up to three tiimes daily. Once your skin has cleared, continue using ZAPZYT to keep new pimples from forming
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZAPZYT ACNE TREATMENT GEL
benzoyl peroxide gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71687-0011 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) DIISOPROPANOLAMINE (UNII: 0W44HYL8T5) LAURETH-4 (UNII: 6HQ855798J) CARBOMER 940 (UNII: 4Q93RCW27E) EDETIC ACID (UNII: 9G34HU7RV0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71687-0011-1 1 in 1 CARTON 12/16/2017 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 12/16/2017 Labeler - Focus Consumer Healthcare, LLC (080743737)