Label: DE-AGING MOISTURIZING DAY CREME WITH SUNSCREEN SPF 20- octinoxate, octisalate, oxybenzone, titanium dioxide cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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  • ACTIVE INGREDIENT

    Active Ingredients                               Purpose Octinoxate 7.5%..............................  Sunscreen Octisalate 3.0%................................  Sunscreen Oxybenzone 3.0%............................. Sunscreen Titanium Dioxide 0.4%.......................Sunscreen



  • PURPOSE

    Uses  Helps prevent sunburn  Higher SPF gives more sunburn protection.

  • Uses

    Helps prevent sunburn.
    Higher SPF gives more sunburn protection.

  • WARNINGS

    Warnings For External use only

  • DO NOT USE

    Do not use on irritated or broken skin.

  • STOP USE

    Stop use and ask a physician if rash, irritation or sensitivity develops and lasts.

  • WHEN USING

    When using this product do not get into eyes, if contact occurs, rinse eyes thoroughly with water.

  • Keep out of reach of chidren.

    In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions  - Apply to clean skin for daily sun protection  - Allow to absorb  - Ask a doctor before use on children under 3 years of age.

  • OTHER SAFETY INFORMATION

    Other Information  Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risks of skin aging, skin cancer and other harmful effects of the sun.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Propylene Glycol, Caprylic/Capric Triglyceride, Glyceryl Stearate, PEG-100 Stearate, Stearic Acid, C12-15 Alkyl Benzoate, Sodium Hyaluronate, Butylene Glycol, Ceramide 2, Human Oligcpeptide-9, Teprenonal, Lonicers Caprifolium (Honeysuckle) Flower Extract, Zizyphus Jujuba Fruit Extract, Glycymhiza Glabra (licorice) Root Extract, Retinyl Palmitate, Tocopheryl Acetate, Cetyl Alcohol Dimethicone, Alumina, Allantein, Panthenol, Sodium PCA, Lecithin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Sodium Phosphate, Sodium Chloride, EDTA, Disodium EDTA, Phenoxyethanol, Caprylyl Glycol, Fragrance.

  • DESCRIPTION

    De-Aging Moisturing Day Creme  With Sunscreen SPF 20  This light and oil-free creme may be used as a base for makeup application. Promotes ultimate hydration for smoother, healthier-looking skin.

  • PRINCIPAL DISPLAY PANEL

    ceLLuLaR laboratories  net vol. 2 fl. oz./60 mL

  • PRINCIPAL DISPLAY PANEL

    Manufactured for and exclusively distributed in the U.S. by: Market America, Inc. 1302 Pleasant Ridge Road Greensboro, NC 27409  Imported and exclusively distributed by: Market Hong Kong, Inc., in Hong Kong  Unit 1615-1620, Level 16, Tower II Grend Century Place 193 Prince Edward Road West Mongkok, Kowloon, Hong Kong.  Market America, Inc., in Canada 100 Wilkinson Road, Unit 5-6 Brampton, Ontario L6T 4Y9.  Market Australia, Inc., in Australia Unit 2/36 Liverpool St. Ingleburn, NSW 2565

  • PRINCIPAL DISPLAY PANEL

    Drug Facts

  • PRINCIPAL DISPLAY PANEL

    Drug Facts (continued)

  • PRINCIPAL DISPLAY PANEL

    Sunscreen 1

  • PRINCIPAL DISPLAY PANEL

    Sunscreen 3

  • PRINCIPAL DISPLAY PANEL

    Sunscreen 4

  • PRINCIPAL DISPLAY PANEL

    Sunscreen 2

  • INGREDIENTS AND APPEARANCE
    DE-AGING MOISTURIZING DAY CREME WITH SUNSCREEN SPF 20 
    octinoxate, octisalate, oxybenzone, titanium dioxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76209-234
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE30 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE4 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CERAMIDE 2 (UNII: C04977SRJ5)  
    JUJUBE FRUIT (UNII: G55HNL2C70)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76209-234-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product12/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/08/2011
    Labeler - Market America (797412236)
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