Label: OLIVIA QUIDO ACNE WASH- benzoyl peroxide liquid
- NDC Code(s): 71421-901-04
- Packager: O Skin Care LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 1, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses
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Warnings
When using this product avoid unnecessary sun exposure and use a sunscreen.
Keep away from eyes, lips, and mouth.
Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occcurs, only one medication should be used unless directed by a doctor. Avoid contact with hair and dyed fabrics, which may be bleached by this product.
- Do not use if you
- Keep out of reach of children
- Directions
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INDICATIONS & USAGE
• 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, apply sunscreen after using this product. If irritation or sensitivity develops, stop use of both products and ask a doctor. -
Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aqua (Water), Bambusa Vulgaris Stem Powder, Butylene Glycol, Carthamus Tinctorius (Safflower) Oleosomes, Ethylhexylglycerin, Glycerin, Jojoba Alcohol, Oleyl Alcohol, PEG-150 Pentaerythrityl Tetrastearate, PEG-6 Caprylic/Capric Glycerides, Phenoxyethanol, Potassium Jojobate, Sodium Cocoyl Isethionate, Sodium Hyaluronate, Sodium Stearoyl Glutamate, Titanium Dioxide, Zanthoxylum Bungeanum Fruit Extract.
- Other Information
- Product Packaging
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INGREDIENTS AND APPEARANCE
OLIVIA QUIDO ACNE WASH
benzoyl peroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71421-901 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 2.5 g in 100 g Inactive Ingredients Ingredient Name Strength PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309) GLYCERIN (UNII: PDC6A3C0OX) ZANTHOXYLUM BUNGEANUM FRUIT (UNII: 3CIP16A418) PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM) BAMBUSA VULGARIS STEM (UNII: SMR633LHTC) OLEYL ALCOHOL (UNII: 172F2WN8DV) PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71421-901-04 120 g in 1 TUBE; Type 0: Not a Combination Product 08/20/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/20/2024 Labeler - O Skin Care LLC (021275401) Registrant - KDC/ONE SOCAL LABORATORIES, LLC (118384240) Establishment Name Address ID/FEI Business Operations KDC/ONE SOCAL LABORATORIES, LLC 118384240 manufacture(71421-901)

