Label: ROC MULTI CORREXION REVIVE AND GLOW MOISTURIZER SPF 30- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 73496-010-00
- Packager: RoC Skincare
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2023
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- OTC Actives
- Uses
- Warnings
- Keep Out of Reach of Children
- Indications and Usage
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Directions For Sunscreen use
Directions For Sunscreen use: • Apply generously and evenly 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water resistant sunscreen if swimming or sweating • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • Limit time in the sun, especially from 10 a.m. – 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses • Children under 6 months of age: Ask a doctor.
- Other information
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Inactive Ingredients
Inactive ingredients Water, Laureth-1, Propanediol, Dimethicone, Alcohol, C12-15 Alkyl Benzoate, Glycerin, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Diethylhexyl 2,6-Naphthalate, 3-O-Ethyl Ascorbic Acid, Butylene Glycol, Citrullus Lanatus (Watermelon) Fruit Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Pyrus Malus (Apple) Fruit Extract, Cistus Monspeliensis Flower/Leaf/Stem Extract, Lens Esculenta (Lentil) Fruit Extract, Sodium PCA, Sodium Lactate, Nonapeptide-1, Lecithin, Silica, Sodium Polyacrylate, Sclerotium Gum, Pullulan, Troxerutin, Polygonum Aviculare Extract, Maltodextrin, Xanthan Gum, Aminomethyl Propanol, Sodium Benzoate, Caprylhydroxamic Acid, Sodium Phosphate, Caprylyl Glycol, Disodium Phosphate, 1,2-Hexanediol, Potassium Sorbate, Fragrance.
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INGREDIENTS AND APPEARANCE
ROC MULTI CORREXION REVIVE AND GLOW MOISTURIZER SPF 30
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73496-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 4 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 5.5 g in 100 mL Inactive Ingredients Ingredient Name Strength POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF) XANTHAN GUM (UNII: TTV12P4NEE) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) WATER (UNII: 059QF0KO0R) WATERMELON (UNII: 231473QB6R) PULLULAN (UNII: 8ZQ0AYU1TT) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) ALCOHOL (UNII: 3K9958V90M) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) APPLE (UNII: B423VGH5S9) CISTUS INCANUS FLOWERING TOP (UNII: N7Z341R6CA) SODIUM LACTATE (UNII: TU7HW0W0QT) NONAPEPTIDE-1 (UNII: 64W45420K5) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) BETASIZOFIRAN (UNII: 2X51AD1X3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) SODIUM BENZOATE (UNII: OJ245FE5EU) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) MALTODEXTRIN (UNII: 7CVR7L4A2D) SODIUM PHOSPHATE (UNII: SE337SVY37) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) DODECYL ETHYLENEGLYCOL MONOETHER (UNII: J89TKQ5R54) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERIN (UNII: PDC6A3C0OX) LENS CULINARIS FRUIT (UNII: ZYZ076G9JH) TROXERUTIN (UNII: 7Y4N11PXO8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73496-010-00 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/01/2023 Labeler - RoC Skincare (117157981) Establishment Name Address ID/FEI Business Operations Dermaceutical Laboratories Limited Liability Company 078457159 manufacture(73496-010)