AVON NUTRA EFFECTS RADIANCE DAY CREAM (OCTINOXATE, OXYBENZONE, HOMOSALATE, AVONBENZONE) CREAM [AVON PRODUCTS, INC.]

AVON NUTRA EFFECTS RADIANCE DAY CREAM (OCTINOXATE, OXYBENZONE, HOMOSALATE, AVONBENZONE) CREAM [AVON PRODUCTS, INC.]
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NDC 71110-0014-1
Set ID 6d99d58a-06e6-8b87-e053-2991aa0aff80
Category HUMAN OTC DRUG LABEL
Packager Avon Products, Inc.
Generic Name
Product Class
Product Number
Application Number PART352
  • ACTIVE INGREDIENT

    Active Ingredients:

    OCTINOXATE 7.5 % ……………………………

    OXYBENZONE 3.5 % ……………………………

    HOMOSALATE 3.0 % ………………………………

    AVOBENZONE 2.5 % ……………………………

  • PURPOSE

    Purpose

    ............Sunscreen

    ............Sunscreen

    ............Sunscreen

    ............Sunscreen

  • INDICATIONS & USAGE

    Uses

    Helps prevent sunburn.

  • WARNINGS

    Warnings

    For external use only.

  • DO NOT USE

    Do not use on damaged or broken skin.

  • WHEN USING

    When using this product, keep out of eyes. Rinse with water to remove.

  • STOP USE

    Stop use and ask a doctor if rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep our of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    For suncreen use:

    Apply liberally and evenly 15 minutes before sun exposure.
    Children under 6 months of age: ask a doctor.
    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-procteion measures, including:
    Limite time in the sun, expecially from 10 a.m.-2 p.m.
    Wear long-sleeved shirts, pants, hats and sunglasses.

  • STORAGE AND HANDLING

    Other Information

    • Protect the product in this container from excessive heat and direct sun,
    • Product may stain fabrics.
  • INACTIVE INGREDIENT

    Inactive ingredients

    WATER/EAU, DIMETHICONE, GLYCERIN, PEG-8, CETEARYL ALCOHOL, TRISILOXANE, BEHENYL ALCOHOL, BUTYLOCTYL SALICYLATE, DILAURYL THIODIPROPIONATE, SILICA, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, DIMETHICONE CROSSPOLYMER, CARBOMER, CETEARETH-20, THIODIPROPIONIC ACID, PHENOXYETHANOL, SODIUM HYDROXIDE, ISOHEXADECANE, CHLORPHENESIN, DISODIUM EDTA, KAEMPFERIA GALANGA ROOT EXTRACT, PARFUM/FRAGRANCE, SODIUM DEHYDROACETATE, POLYSORBATE 60, PANTHENOL, STRELITZIA NICOLAI SEED ARIL EXTRACT, TOCOPHERYL ACETATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, SALVIA HISPANICA SEED EXTRACT, MALTODEXTRIN, POUZOLZIA PENTANDRA EXTRACT.

  • PRINCIPAL DISPLAY PANEL

    image of PDPimage of DFB

  • INGREDIENTS AND APPEARANCE
    AVON NUTRA EFFECTS  RADIANCE DAY CREAM
    octinoxate, oxybenzone, homosalate, avonbenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71110-0014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE30 mg  in 1 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE25 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE35 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DILAURYL THIODIPROPIONATE (UNII: V51YH1B080)  
    SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    THIODIPROPIONIC ACID (UNII: 3BBK323ED8)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71110-0014-11.1 g in 1 PACKET; Type 0: Not a Combination Product03/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35203/01/2016
    Labeler - Avon Products, Inc. (001468693)
    Establishment
    NameAddressID/FEIBusiness Operations
    Avon Manufacturing (Guangzhou) Ltd544863277manufacture(71110-0014)

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