Label: GOOD SKIN MD FACIAL MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15- zinc oxide lotion

  • NDC Code(s): 69423-692-50
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 6, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    ZINC OXIDE 9.7%

    Sunscreen

  • Uses

    • helps 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 use

    • on damaged or broken skin

    When using this product

    • keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor if

    • rash occurs

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

  • Directions

    • shake well before use
    • apply liberally 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use 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 sun, especially from 10 a.m. – 2 p.m.
      • wear long-sleeved shirts, pants, hats, and sunglasses
    • children under 6 months: ask a doctor
  • Other information

    • protect this product from excessive heat and direct sun
  • Inactive ingredients

    Water, caprylic/capric triglyceride, isohexadecane, glycerin, hydroxyacetophenone, C13-14 isoparaffin, steareth-21, polyhydroxystearic acid, laureth-7, steareth-2, stearyl alcohol, behenyl alcohol, cetyl alcohol, disodium EDTA, polyacrylamide, triethoxycaprylylsilane, phenoxyethanol.

  • SPL UNCLASSIFIED SECTION

    Distr. by: PROCTER & GAMBLE

    CINCINNATI, OH 45202

    www.getgoodskinmd.com

  • Questions & comments?

    Questions or comments? 888-FAB-3063

  • PRINCIPAL DISPLAY PANEL - 50 mL Carton

    GOOD SKIN MD

    DERMATOLOGIST TESTED

    Facial Moisturizer

    with SUNSCREEN

    ZINC OXIDE

    BROAD SPECTRUM

    SPF 15

    50 mL (1.7 FL OZ)

    GS

  • INGREDIENTS AND APPEARANCE
    GOOD SKIN MD FACIAL MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 15 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-692
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE9.7 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LAURETH-7 (UNII: Z95S6G8201)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    STEARETH-21 (UNII: 53J3F32P58)  
    STEARETH-2 (UNII: V56DFE46J5)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-692-501 in 1 CARTON03/01/2022
    150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02003/01/2022
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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