OLIVIA QUIDO ACNE WASH- benzoyl peroxide liquid

Olivia Quido Acne Wash by

Drug Labeling and Warnings

Olivia Quido Acne Wash by is a Otc medication manufactured, distributed, or labeled by O Skin Care LLC, KDC/ONE SOCAL LABORATORIES, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzoyl Peroxide 2.5%

PURPOSE

Acne Treatment

Uses

For the treatment of acne

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

Have very sensitive skin

Are sensitive to Benzoyl Peroxide

Keep out of reach of children

If product is swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Wet affected area, wash, and rinse well.

Use once or twice daily or as directed by a physician.

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

Store at controlled temperature: 15°C -30°C
(59°F-86°F), away direct sunlight.

Product Packaging

INGREDIENTS AND APPEARANCE

OLIVIA QUIDO ACNE WASH 
benzoyl peroxide liquid

Product 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)