METHOD MEN FACE WITH ZINC OXIDE SUNSCREEN- zinc oxide lotion

Method Men Face with Zinc Oxide Sunscreen by

Drug Labeling and Warnings

Method Men Face with Zinc Oxide Sunscreen by is a Otc medication manufactured, distributed, or labeled by Method Products Inc., AUTUMN HARP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • PRINCIPAL DISPLAY PANEL - 74 mL Bottle Carton

    method®
    men

    FACE LOTION
    WITH ZINC OXIDE SUNSCREEN
    BROAD SPECTRUM SPF 15

    infused with vitamin E
    + hemp seed oil

    fragrance free

    74 mL (2.5 FL OZ)

    PRINCIPAL DISPLAY PANEL - 74 mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    METHOD MEN FACE WITH ZINC OXIDE SUNSCREEN 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 52494-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)  
    POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    JOJOBA OIL (UNII: 724GKU717M)  
    SUCROSE COCOATE (UNII: 3H18P0UK73)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    1-PALMITOYL-2-LINOLEOYL-SN-GLYCERO-3-PHOSPHOCHOLINE (UNII: 6UCA7I41S8)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 52494-100-2574 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/10/202112/31/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM02001/10/202112/31/2026
    Labeler - Method Products Inc. (036514797)
    Establishment
    NameAddressID/FEIBusiness Operations
    AUTUMN HARP064187883MANUFACTURE(52494-100)

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