Label: SERIOUS SKINCARE CONTINUOUSLY CLEAR CLEARZ IT- benzoyl peroxide cream
- NDC Code(s): 53755-392-00
- Packager: Flageoli Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 5, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
-
Warnings
• For external use only.
Keep this and all medications out of the reach of children.
• 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 excessive skin irritation develops or increases, discontinue use and see a doctor. • Only one medication should be used unless directed by a doctor. • Do not get into eyes. • In case of accidental ingestion, seek professional assistance or contact: Poison Control Center immediately. • Peroxide can bleach hair and dyed fabrics.
-
Directions
• Shake well before applying to freshly cleansed skin. • Because excessive drying may occur, apply one thin layer daily, then increase application to two to three times daily. • If excessive dryness or peeling occurs, reduce application to once a day or every other day. • Avoid contact with eyes, eyelids or mucus membranes. • Store in cool dry place.
-
Inactive ingredients
Water, Glycerin, Melaleuca Alternifiolia (Tea Tree) Leaf Oil, Camellia Sinesis Leaf Extract, Butylene Glycol, Sodium PCA, Betaine, Sorbitol, Glycine, Alanine, Proline, Serine, Threonine, Arginine, Lysine, Glutamic Acid, Allantoin, Disodium EDTA, Carbomer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Phenoxyethanol, Methylparaben, Butlyparaben, Ethylparaben, Propylparaben, Isobutylparaben.
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
SERIOUS SKINCARE CONTINUOUSLY CLEAR CLEARZ IT
benzoyl peroxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53755-392 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TEA TREE OIL (UNII: VIF565UC2G) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) BETAINE (UNII: 3SCV180C9W) SORBITOL (UNII: 506T60A25R) GLYCINE (UNII: TE7660XO1C) ALANINE (UNII: OF5P57N2ZX) PROLINE (UNII: 9DLQ4CIU6V) SERINE (UNII: 452VLY9402) THREONINE (UNII: 2ZD004190S) ARGININE (UNII: 94ZLA3W45F) LYSINE (UNII: K3Z4F929H6) GLUTAMIC ACID (UNII: 3KX376GY7L) ALLANTOIN (UNII: 344S277G0Z) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYLPARABEN (UNII: 3QPI1U3FV8) ETHYLPARABEN (UNII: 14255EXE39) PROPYLPARABEN (UNII: Z8IX2SC1OH) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53755-392-00 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/27/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 02/27/2023 Labeler - Flageoli Limited (036999498)