Label: FIRST AID BEAUTY FAB WEIGHTLESS MINERAL SUNSCREEN BROAD SPECTRUM SPF 30- zinc oxide liquid

  • NDC Code(s): 69423-690-44
  • 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 July 27, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Zinc oxide 22%

    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

    Ethylhexyl Olivate, Isododecane, Coconut Alkanes, Aluminum Starch Octenylsuccinate, Caprylic/Capric Triglyceride, Water (Aqua), Butylene Glycol, Polyglyceryl-6 Polyricinoleate, Jojoba Esters, Cellulose, Stearalkonium Hectorite, Sodium Chloride, Squalane, Polyglyceryl-3 Polyricinoleate, Polyglyceryl-3 Diisostearate, Phenoxyethanol, Tocopheryl Acetate, Coco-Caprylate/Caprate, Trihydroxystearin, Caprylyl Glycol, Polyhydroxystearic Acid, Trisodium Ethylenediamine Disuccinate, Glycerin, Glycyrrhiza Glabra (Licorice) Root Extract, Propanediol, Sorbic Acid, Silica, Camellia Sinensis Leaf Extract, Chrysanthemum Parthenium (Feverfew) Extract, Alumina, Tocopherol, Mica (CI 77019), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499), Titanium Dioxide (CI 77891)

  • Questions?

    888-FAB-3063

  • SPL UNCLASSIFIED SECTION

    MADE IN USA.

    FIRST AID BEAUTY ® LTD
    NEWTON, MA 02458.

    WWW.FIRSTAIDBEAUTY.COM

  • PRINCIPAL DISPLAY PANEL

    FIRST AID BEAUTY ​®

    FAB

    Weightless Liquid Mineral

    Sunsceren

    with Zinc Oxide

    Broad Spectrum SPF 30

    1.5 FL OZ (44 mL)

    FAB

  • INGREDIENTS AND APPEARANCE
    FIRST AID BEAUTY FAB WEIGHTLESS MINERAL SUNSCREEN BROAD SPECTRUM SPF 30 
    zinc oxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-690
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE22 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K)  
    POLYGLYCERYL-10 POLYRICINOLEATE (UNII: DHM1T5XO11)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    MICA (UNII: V8A1AW0880)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    COCONUT ALKANES (UNII: 1E5KJY107T)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    ISODODECANE (UNII: A8289P68Y2)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIHYDROXYSTEARIN (UNII: 06YD7896S3)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SQUALANE (UNII: GW89575KF9)  
    POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SORBIC ACID (UNII: X045WJ989B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-690-441 in 1 CARTON05/10/2023
    144 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM02005/01/2023
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!