Label: GLOW GO LIP OIL- avobenzone 30mg/g, homosalate 100mg/g, octocrylene 100mg/g, octisalate 50mg/g, oil
- NDC Code(s): 81104-800-01
- Packager: NAKED SUNDAY PTY LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 26, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USE
- WARNINGS
- WHEN USING
- Stop use & ask doctor
- KEEP OUT OF REACH OF CHILDREN
- Directions
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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
- OTHER SAFETY INFORMATION
- DOSAGE & ADMINISTRATION
- Label
-
INGREDIENTS AND APPEARANCE
GLOW GO LIP OIL
avobenzone 30mg/g, homosalate 100mg/g, octocrylene 100mg/g, octisalate 50mg/g, oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81104-800 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 mL Inactive Ingredients Ingredient Name Strength ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) MICA (UNII: V8A1AW0880) POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7) CANDELILLA WAX (UNII: WL0328HX19) CITRULLUS LANATUS WHOLE (UNII: 3J5I6254YO) PHENOXYETHANOL (UNII: HIE492ZZ3T) OCTYLDODECANOL (UNII: 461N1O614Y) SOLANUM LYCOCARPUM FRUIT (UNII: GL29VWX729) SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81104-800-01 4.5 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/07/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/07/2022 Labeler - NAKED SUNDAY PTY LTD (746918845)