Label: GLOW BODY MIST SPF 50- avobenzone, homosalate, octisalate, octocrylene spray
- NDC Code(s): 30807-5005-1
- Packager: WILD CHILD LABORATORIES PTY LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 24, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- USE
- warning
- When using this product
- stop use and ask a doctor
- Keep Out of reach of children
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Directions
Generously spray to exposed areas holding bottle 10-15 cm away from skin. Ensure even application by spraying at least 7 times per section of body until product is visible, Rub in lightly.
Use a water- resistant sunscreen if swimming or sweating.
reapply at least every 2 hours.
Children under 6 months of age : ask a doctor
- Inactive Ingredients
- other information
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Sun Protection Measures
Spending time in the Sun Increases your risk of skin cancer and early skin ageing. 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 the sun, especially from 10.00 AM - 2.00 PM
Wea long-sleeved Shirts , pants hats, and sunglasses,
- Purpose
- Purpose
- Label
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INGREDIENTS AND APPEARANCE
GLOW BODY MIST SPF 50
avobenzone, homosalate, octisalate, octocrylene sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30807-5005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10.5 g in 100 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 4.5 g in 100 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 15 g in 100 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 7.5 g in 100 mL Inactive Ingredients Ingredient Name Strength KAKADU PLUM (UNII: 0ZQ1D2FDLI) ALCOHOL (UNII: 3K9958V90M) WATERMELON SEED OIL (UNII: L33J06UQTT) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30807-5005-1 150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 09/01/2021 Labeler - WILD CHILD LABORATORIES PTY LTD (890661643)