Label: GLOW GO LIP OIL- avobenzone 30mg/g, homosalate 100mg/g, octocrylene 100mg/g, octisalate 50mg/g, oil

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 25, 2024

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

View All Sections
  • ACTIVE INGREDIENTS

    AVOBENZONE 3 %

    HOMOSALATE 10%

    OCTISALATE 5 %

    OCTOCRYLENE 10%

  • PURPOSE

    SUNSCREEN

  • USE

    - Helps prevents sunburn

    - If used as directed with other sun protection measures ( see directions) decreases the risk of skin cancer and early skin ageing caused by the sun.

  • WARNINGS

    FOR EXTERNAL USE ONLY

    - Do not use on damaged or broken skin.

  • WHEN USING

    keep out of eyes, Rinse with water to remove

  • Stop use & ask 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

    - Apply 20 minutes before sun exposure

    - Use a water resistant sunscreen if swimming or sweating

    - Re-apply frequently especially after swimming excercising or towel drying

    - Re-apply at least every 2 hours

    - Children under 6 months of age- ask a doctor

  • 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 inclusing:

    - limit time in the sun, especially from 10:00 AM- 02:00 PM

    - Wear long- Sleeved shirts , pants, Hats and sunglasses

  • Inactive Ingredients

    Candelilla wax, Citrullus Lanatus Seed oil, Flavor, Isopropyl myristate, MICA, Octyldodecanol, Phenoxyethanol, Polybutene, Simmondsis Chinensis (jojoba) seed oil, Solanum Lycopersicum (Tomato) fruit extract,

  • OTHER SAFETY INFORMATION

    Protect the product in this container from excessive heat & direct sun

  • DOSAGE & ADMINISTRATION

  • DOSAGE & ADMINISTRATION

    - Apply 20 minutes before sun exposure

    - Use a water resistant sunscreen if swimming or sweating

    - Re-apply frequently especially after swimming excercising or towel drying

    - Re-apply at least every 2 hours

    - Children under 6 months of age- ask a doctor

  • Label

    21

  • INGREDIENTS AND APPEARANCE
    GLOW GO LIP OIL 
    avobenzone 30mg/g, homosalate 100mg/g, octocrylene 100mg/g, octisalate 50mg/g, oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81104-600
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 mL
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    MICA (UNII: V8A1AW0880)  
    CANDELILLA WAX (UNII: WL0328HX19)  
    CITRULLUS LANATUS WHOLE (UNII: 3J5I6254YO)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
    SOLANUM LYCOCARPUM FRUIT (UNII: GL29VWX729)  
    JOJOBA OIL (UNII: 724GKU717M)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81104-600-014.5 mL in 1 BOTTLE; Type 0: Not a Combination Product08/07/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/07/2022
    Labeler - NAKED SUNDAY PTY LTD (746918845)
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!