Label: PLAY SUNSCREEN SPF 50- homosalate, octocrylene, octisalate, avobenzone stick
- NDC Code(s): 75936-649-01
- Packager: Supergoop LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 3, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- INDICATIONS & USAGE
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DOSAGE & ADMINISTRATION
Apply generously and evenly 15 minutes before sun exposure
Reapply (will vary depending on WR)
after XX minutes of swimming or sweating
Immediately after towel drying
at least every 2 hours
Use a water resistant sunscreen if swimming or sweating
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
Ethylhexyl Palmitate, Synthetic Wax, Tapioca Starch, Butyloctyl Salicylate, Silica, Cocos Nucifera (Coconut) Oil, Helianthus Annuus (Sunflower) Seed Oil, Tocopherol, Orange Oil Terpenes, Eucalyptus Globulus Leaf Oil, Citrus Limon (Lemon) Peel Oil, Pelargonium Graveolens Flower Oil, Glycine Soja (Soybean) Oil, Aniba Rosaeodora (Rosewood) Wood Oil, Pogostemon Cablin Oil, Ocimum Basilicum (Basil) Oil, Limonene.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PLAY SUNSCREEN SPF 50
homosalate, octocrylene, octisalate, avobenzone stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75936-649 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 7 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 7 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SUNFLOWER OIL (UNII: 3W1JG795YI) ORANGE TERPENES (UNII: 9J3RG7FX7S) POGOSTEMON CABLIN OIL (UNII: F3IN55X5PO) ETHYLHEXYL PALMITATE (UNII: 2865993309) TOCOPHEROL (UNII: R0ZB2556P8) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) COCONUT OIL (UNII: Q9L0O73W7L) CITRUS LIMON (LEMON) PEEL OIL (UNII: I9GRO824LL) STARCH, TAPIOCA (UNII: 24SC3U704I) ANIBA ROSAEODORA WOOD (UNII: NE01NKA8B2) PARAFFIN (UNII: I9O0E3H2ZE) SOYBEAN OIL (UNII: 241ATL177A) OCIMUM BASILICUM (BASIL) OIL (UNII: Z129UMU8LE) EUCALYPTUS OIL (UNII: 2R04ONI662) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75936-649-01 40 g in 1 TUBE; Type 0: Not a Combination Product 03/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/03/2024 Labeler - Supergoop LLC (117061743)
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