Label: GLOW STICK BROAD SPECTRUM SPF 50- avobenzone, octisalate, octocrylene stick
- NDC Code(s): 75936-157-02
- Packager: Supergoop, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 14, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
- Apply generously and evenly 15 minutes before sun exposure
Reapply:
- After 40 minutes of swimming or sweating
- Immediately after towel drying
- At least every 2 hours
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 including:
- Limit time in the sun, especially from 10 a.m. - 2 p.m.
- Wear long-sleeved shirts, pants, hats and sunglasses
- Children under 6 months: ask a doctor
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INACTIVE INGREDIENT
Inactive Ingredients
Caprylic/Capric Triglyceride, Octyldodecanol, Isododecane, Isohexadecane, Dicaprylyl Carbonate, C12-15 Alkyl Benzoate, Dibutyl Lauroyl Glutamide, Polyester-8, Dibutyl Ethylhexanoyl Glutamide, Diethylhexyl Syringylidenemalonate, Helianthus Annuus (sunflower) Seed Oil, Pentaclethra Macroloba Seed Oil, Maurita Flexuosa Fruit Oil, Limnanthes Alba (Meadowfoam) Seed Oil, Callophyllum Inophyllum seed Oil, Calendula Officinalis Extract, Tocopherol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GLOW STICK BROAD SPECTRUM SPF 50
avobenzone, octisalate, octocrylene stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75936-157 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 g Inactive Ingredients Ingredient Name Strength TOCOPHEROL (UNII: R0ZB2556P8) SUNFLOWER OIL (UNII: 3W1JG795YI) ISOHEXADECANE (UNII: 918X1OUF1E) TAMANU OIL (UNII: JT3LVK84A1) ISODODECANE (UNII: A8289P68Y2) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X) OCTYLDODECANOL (UNII: 461N1O614Y) MEADOWFOAM SEED OIL FATTY ACIDS (UNII: MK2D1PBV6N) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P) DIBUTYL ETHYLHEXANOYL GLUTAMIDE (UNII: 0IAF2L30VS) DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248) PENTACLETHRA MACROLOBA SEED OIL (UNII: OM0BAV5397) MAURITIA FLEXUOSA FRUIT OIL (UNII: 48H19MS04L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75936-157-02 35 g in 1 CYLINDER; Type 0: Not a Combination Product 03/09/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/03/2018 Labeler - Supergoop, LLC (117061743)
