- Drug Facts
- Use
- Warnings
-
When using this product
- Skin irritation and dryness are more likely to occur if you use another topical acne medication at the same time (if irritation occurs, use only one topcial 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 byusing the product less frequently or in a lower concentration.
- Do Not Use
- Stop use and ask a doctor
- Keep out of reach of children.
-
Directions
Sensitivity test for a new user: Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, apply the acne wash and gently massage into damp skin. Wait 3 to 5 minutes to absorb, and then thoroughly rinse area with water. If going outside, apply sunscreen after using this product. If irritation or sensitivity develops stop use and ask a doctor.
- Other Ingredients
- Distributed by
- PDP
-
INGREDIENTS AND APPEARANCE
KIVORIA ACNE WASH
benzoyl peroxide soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71131-100 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 ASCORBIC ACID (UNII: PQ6CK8PD0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) THYMUS VULGARIS LEAF (UNII: GRX3499643) WATER (UNII: 059QF0KO0R) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CARBOMER 934 (UNII: Z135WT9208) GLUCONOLACTONE (UNII: WQ29KQ9POT) HYDROXIDE ION (UNII: 9159UV381P) ALOE VERA LEAF (UNII: ZY81Z83H0X) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71131-100-08 1 in 1 BOX 04/01/2019 1 226 g in 1 BOTTLE; 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 04/01/2019 Labeler - UberScientific, LLC (080459429) Registrant - UberScientific, LLC (080459429)