Label: ALBA SUNBLOCK FACIAL SPF 20- zinc oxide, titanium dioxide cream

  • Category: HUMAN OTC DRUG LABEL

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 June 25, 2010

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS

    Zinc Oxide  8.0%

    Titanium Dioxide  1.0%

  • INDICATIONS & USAGE

                  USES

    • Helps prevent sunburns
    • Higher SPF gives more sunburn protection
    • Apply liberally before sun exposure as needed
    • Reapply as needed or after swimming, perspiring or towel drying
    • Children under 6 months of age: ask doctor
  • WARNINGS

    WARNINGS

    For external use only. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash or irritation develops and lasts. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

  • QUESTIONS

    QUESTIONS?

    Call (888) 659-7730 or visit www.AlbaBotanica.com

    100% Vegetarian Ingredients

    No Animal Testing

    Alba Botanica

    The Hain Celestial Group, Inc.

    Melville, NY 11747

    Made in the U.S.A.


  • PRINCIPAL DISPLAY PANEL

    image of tube label
  • INGREDIENTS AND APPEARANCE
    ALBA SUNBLOCK FACIAL SPF 20 
    zinc oxide, titanium dioxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61995-2387
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Cation - UNII:13S1S8SF37) Zinc Oxide8.0 g  in 100 g
    Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide1.0 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61995-2387-4113 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35210/28/2009
    Labeler - The Hain Celestial Group, Inc. (858894996)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Hain Celestial Group, Inc.858894996manufacture