DYNAMIC BROAD SPECTRUM SUNSCREEN SPF 55- octinoxate and zinc oxide cream

Dynamic Broad Spectrum Sunscreen SPF 55 by

Drug Labeling and Warnings

Dynamic Broad Spectrum Sunscreen SPF 55 by is a Otc medication manufactured, distributed, or labeled by Prescriber's Choice, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • INACTIVE INGREDIENTS

    Water, Hydrogenated Polybutene, Octyl Stearate, Polyglyceryl-4-Isostearate, Aloe Barbadensis Leaf Extract, Isopropyl Palmitate, Cyclomethicone, Sunflower Oil, Hydrogenated Microcrystalline Wax, Cetyl Dimethicone Copolyol, Cetyl Dimethicone, Hydrogenated Castor Oil, Sodium Chloride, Polyglyceryl-3-Oleate, Silica, Hexyl Laurate, Triethoxycaprylylsilane, Capryly Glycol, Methylisothiazolinone.

  • OTHER INFORMATION

    Store at controlled temperature 15C – 30C (59F-86F). Protect the product in this container from excessive heat and direct sun.

  • Prescriber's Choice, LLC Dynamic Broad Spectrum Sunscreen SPF 55 1.75 fl oz (50ml)

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  • INGREDIENTS AND APPEARANCE
    DYNAMIC BROAD SPECTRUM SUNSCREEN SPF 55 
    octinoxate and zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 71876-5550
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE48 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOCETYL STEARATE (UNII: 3RJ7186O9W)  
    SORBITOL (UNII: 506T60A25R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    ALCOHOL (UNII: 3K9958V90M)  
    OCTISALATE (UNII: 4X49Y0596W)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    BETULA PUBESCENS BARK (UNII: 3R504894L9)  
    GARDEN CRESS SPROUT (UNII: PWQ18YNR62)  
    SAGE (UNII: 065C5D077J)  
    COLA ACUMINATA SEED (UNII: 1F8VIW1479)  
    CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ISOMALT (UNII: S870P55O2W)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 71876-5550-250 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/08/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35201/08/2021
    Labeler - Prescriber's Choice, LLC (038962843)

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