Label: ALOE UP LIGHT TANNING OIL SPF-6- avobenzone, octyl salicylate, homosalate, octocrylene spray

  • NDC Code(s): 61477-226-24
  • Packager: Aloe Care International, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 13, 2024

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

View All Sections
  • ACTIVE INGREDIENTS:

    Avobenzone (1.0%)

    Octyl Salicylate (3.0%)

    Homosalate (1.0%)

    Octocrylene (.85%)

  • PURPOSE:

    SUNSCREEN

  • USES

    HELPS PREVENT SUNBURN.

  • DIRECTIONS:

    • Apply liberally. Reapply after swimming or after excessive sweating.

  • KEEP OUT OF REACH OF CHILDREN

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

  • WARNINGS:

    Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.
    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.
    Keep away from face to avoid breathing it. Contents under pressure - do not puncture or incinerate. Do not store at temperatures above 120°F.
    Stop use and ask a doctor if rash occurs

    Flammable: Do not use near heat, flame or while smoking.

  • INACTIVE INGREDIENTS

    Aloe Oil Extract, Coconut Oil, Palm Oil, Banana Oil, Apricot Oil, Almond Oil, Tocopheryl Acetate (Vitamin E).

  • OTHER INFORMATION

    • Protect this product from excessive heat and direct sun

  • Questions or comments?

    Toll Free 800-950-2563 www.aloeup.com

  • PRINCIPAL DISPLAY PANEL

    LBL_Aloe Up Light Tanning Oil SPF-6

  • INGREDIENTS AND APPEARANCE
    ALOE UP LIGHT TANNING OIL  SPF-6
    avobenzone, octyl salicylate, homosalate, octocrylene spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61477-226
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE3 g  in 100 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE1 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE0.85 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PALM OIL (UNII: 5QUO05548Z)  
    BANANA (UNII: 4AJZ4765R9)  
    APRICOT KERNEL OIL (UNII: 54JB35T06A)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61477-226-24120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/17/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/17/2019
    Labeler - Aloe Care International, LLC (938242187)
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

More Info on this Drug

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