Label: SALT AND STONE SUNSCREEN LIP BALM SPF 30- zinc oxide stick
- NDC Code(s): 71585-139-00
- Packager: Salt and Stone LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 28, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
- Apply liberally 15 minutes before sun exposure
- Reapply:
- • After 80 minutes of swimming or sweating • Immediately after towel drying •At Least every 2 hours
- Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • Limit time in the sun, especially from 10am - 2pm. • Wear long-sleeved shirts, pants, hats, and sunglasses.
Sun Protection Measures.
- Children under 6 months: Ask a doctor
- Other Information
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Inactive Ingredients
Prunus Amygdalus Dulcis (Sweet Almond) Oil, Butyrospermum Parkii (Shea) Butter, Cera Flava (Beeswax), Simmondsia Chinensis (Jojoba) Seed Oil, Euphorbia Cerifera (Candelilla) Wax, Tocopheryl Acetate, Argania Spinosa Kernel (Argan) Oil, Copernicia Cerifera (Carnauba) Wax, Tocopherol, Glycine Soja (Soybean) Oil, Bisabolol, GlycerylCaprylate, Glyceryl Undecylenate, Triethoxycaprylylsilane
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SALT AND STONE SUNSCREEN LIP BALM SPF 30
zinc oxide stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71585-139 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.08 g in 1 g Inactive Ingredients Ingredient Name Strength ALMOND OIL (UNII: 66YXD4DKO9) SHEA BUTTER (UNII: K49155WL9Y) CANDELILLA WAX (UNII: WL0328HX19) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARNAUBA WAX (UNII: R12CBM0EIZ) TOCOPHEROL (UNII: R0ZB2556P8) SOYBEAN OIL (UNII: 241ATL177A) LEVOMENOL (UNII: 24WE03BX2T) GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A) GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71585-139-00 4.3 g in 1 APPLICATOR; Type 0: Not a Combination Product 11/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/23/2020 Labeler - Salt and Stone LLC (080683697)