Label: PLAY SPF 30 LIP SHIELD COCONUT- avobenzone, homosalate, octisalate, octocrylene gel
- NDC Code(s): 75936-156-01
- Packager: Supergoop, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 16, 2024
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
-
DOSAGE & ADMINISTRATION
Apply generously and evenly 15 minutes before sun exposure.
- reapply: after 80 minutes of swimming or sweating.
- immediately after towel drying
- at least every 2 hours
- Sun Protection Measures: Spending time in the sun increases your skin 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
-
INACTIVE INGREDIENT
Butyloctyl Salicylate, Butyrospermum Parkii (Shea) Butter, Cocos Nucifera (Coconut) Oil, Euphorbia Cerifera (Candelila) Wax, Flavor (Coconut), Aloe Barbadensis Leaf Extract, Helianthus Annuus (Sunflower) Seed Oil, Ozokeite Wax, Persea Gratissima (Avocado) Oil, Rosmarinus Officinalis (Rosemary) Leaf Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Stevia Rebaudiana Extract, Tocopherol, Vitis Vinifera (Grape) Seed Oil
- STORAGE AND HANDLING
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
PLAY SPF 30 LIP SHIELD COCONUT
avobenzone, homosalate, octisalate, octocrylene gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75936-156 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 OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) SHEA BUTTER (UNII: K49155WL9Y) COCONUT OIL (UNII: Q9L0O73W7L) CANDELILLA WAX (UNII: WL0328HX19) ALOE VERA LEAF (UNII: ZY81Z83H0X) CERESIN (UNII: Q1LS2UJO3A) SUNFLOWER OIL (UNII: 3W1JG795YI) AVOCADO OIL (UNII: 6VNO72PFC1) JOJOBA OIL (UNII: 724GKU717M) TOCOPHEROL (UNII: R0ZB2556P8) GRAPE SEED OIL (UNII: 930MLC8XGG) ROSEMARY (UNII: IJ67X351P9) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75936-156-01 4.25 g in 1 TUBE; Type 0: Not a Combination Product 10/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/02/2020 Labeler - Supergoop, LLC (117061743)