Label: CLEAR COMPLEXION ACNE SERUM- benzoyl peroxide serum cream
- NDC Code(s): 70809-1903-1
- Packager: USRX LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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PRINCIPAL DISPLAY PANEL
- Warning For external use only
- When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water.
- Stop and ask a doctor if rash or irritation develops and lasts.
Directions: Thoroughly cleanse face and pat dry. Apply to face and neck area for an all over acne treatment or apply directly to the breakout/pimple for a fast acting spot treatment. Can be used 1-2 times daily or for sensitive skin types use every other night. If dryness or irritation occurs, reduce amount of applications.
WATER, GLYCOLIC ACRYLATESCOPOLYMER, OLIGOPEPTI KOJICACID, RETINOLPALMITATE, TOCO JUICE, SALIXNIGRA(WILLOW) BARKEX HAZEL) WATER, ARNICAMONTANA(AR ACID, ZINC OXIDE, (ORGANIC) ECHI FICUS-INDICASTEMEXTRACT, (ORGA SODIUMPHYTATE, ALCOHOL, BUTYLEN SODIUMOLEATE, DISODIUMEDTA, SO POLYISOBUTENE, POLYSORBATE20, AM COPOLYMER, PHENOXYETHANOL, ETH CARBOMER, DIMETHICONE, PEG-40 SODIUM DIOCTYL SULFOSUCCINATE, SORBITAN ISOSTEARATE, BENZOIC A
ACID, PROPANEDIOL, GLYCERIN, SODIUM DE-68, ALPHA-ARBUTIN, GLUTATHIONE, PHEROLOIL, ALOEBARBADENSISLEAF TRACT, HAMAMELISVIRGINIANA(WITCH NICA) EXTRACT, NIACINAMIDE, AZELAIC NACEAANGISTIFOLIAROOT, OPUNTIA NIC) ALCOHOL, CITRICACID, LECITHIN, EGLYCOL, HYDROGENATEDLECITHIN, DIUMHYDROXIDE, POLYACRYLATE-13, MONIUMACRYLOYLDIMETHYLTAURATE/VP YLHEXYLGLYCERIN, 1,3PROPANEDIOL, STEARATE, SILICA, SODIUM CITRATE, SORBITAN STEARATE, XANTHAN GUM,
CID, GLYCINE SOJA (SOYBEAN) OIL. -
INGREDIENTS AND APPEARANCE
CLEAR COMPLEXION ACNE SERUM
benzoyl peroxide serum creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70809-1903 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 7.5 mg in 100 mL Inactive Ingredients Ingredient Name Strength GLYCOLIC ACID (UNII: 0WT12SX38S) PROPANEDIOL (UNII: 5965N8W85T) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70809-1903-1 120 mL in 1 TUBE; Type 0: Not a Combination Product 07/08/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/08/2019 Labeler - USRX LLC (115270633) Registrant - USRX LLC (115270633)