Label: SERIOUSLY SOOTHING SPF DAY CREAM- zinc oxide cream

  • NDC Code(s): 54136-179-52
  • Packager: Better Planet Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 3, 2025

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  • Active ingredients

    Zinc Oxide 15.50%

  • Purpose

    Sunscreen

  • Uses

    * Help prevent sunburn * if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • Warnings

    For external use only.

    Do not useon damaged or broken skin.

    When using the product* keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctorif rash occurs.

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

    May stain some fabrics.

  • Directions

    • apply liberally 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-sleeveshirts, pants, hats, and sunglasses

  • Other information

    Protect this product from excessive heat and direct sun. • May stain some fabrics.

  • Inactive Ingredients

    WATER, COCO-CAPRYLATE/CAPRATE, CELEARYL OLIVATE, SORBITAN OLIVATE, NIACINAMIDE, PANTHENOL, TOCOPHERYL ACETATE, TANACETUM ANNUUM FLOWER OIL, LAUROYL LYSINE, LECITHIN, PULLULAN, SCLEROTIUM GUM, XANTHAN GUM, CETEARYL ALCOHOL, POLYHYDROXYSTEARIC ACID, SILICA, SODIUM PHYTATE, DEHYDROACETIC ACID, BENZYL ALCOHOL

  • Questions?

    Call toll-free 877.902.2873

  • PRINCIPAL DISPLAY PANEL

    Box

  • INGREDIENTS AND APPEARANCE
    SERIOUSLY SOOTHING SPF DAY CREAM 
    zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54136-179
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LAUROYL LYSINE (UNII: 113171Q70B)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    TANACETUM ANNUUM FLOWERING TOP OIL (UNII: E2Q02N1ZC7)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    BETASIZOFIRAN (UNII: 2X51AD1X3T)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PULLULAN (UNII: 8ZQ0AYU1TT)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    HEXASODIUM PHYTATE (UNII: ZBX50UG81V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54136-179-5252 g in 1 TUBE; Type 0: Not a Combination Product04/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02004/01/2024
    Labeler - Better Planet Brands LLC (960253719)
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