Label: PLAY MINERAL SUNSTICK SPF-30- zinc oxide stick
- NDC Code(s): 73088-102-11
- Packager: TUBBY TODD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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DIRECTIONS
• Apply generously 15 minutes before sun exposure and as needed.
• reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating.
• Children under 6 months of age: ask a doctor
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. [bullet] wear long-sleeved shirts, pants, hats, and sunglasses". - OTHER INFORMATION
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INACTIVE INGREDIENT
Cocos Nucifera (Coconut) Oil*, Helianthus Annuus (Sunflower) Seed Oil*,Cera Alba (Beeswax)*,Euphorbia Cerifera Cera (Candelilla Wax),Copernicia Cerifera (Carnauba) Wax*, Butyrospermum Parkii (Shea) Butter*, Ricinus Communis (Castor) Seed Oil*,Tocopherol, Theobroma Cacao (Cocoa) Seed Butter*,Aloe Barbadensis Leaf Juice (Aloe Vera)* *Organic
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PLAY MINERAL SUNSTICK SPF-30
zinc oxide stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73088-102 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 20 g in 100 g Inactive Ingredients Ingredient Name Strength SUNFLOWER OIL (UNII: 3W1JG795YI) YELLOW WAX (UNII: 2ZA36H0S2V) COCONUT OIL (UNII: Q9L0O73W7L) CANDELILLA WAX (UNII: WL0328HX19) CARNAUBA WAX (UNII: R12CBM0EIZ) SHEA BUTTER (UNII: K49155WL9Y) CASTOR OIL (UNII: D5340Y2I9G) TOCOPHEROL (UNII: R0ZB2556P8) COCOA BUTTER (UNII: 512OYT1CRR) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73088-102-11 14 g in 1 TUBE; Type 0: Not a Combination Product 05/21/2019 12/12/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/21/2019 12/12/2024 Labeler - TUBBY TODD (052545299)