Label: SALT AND STONE NATURAL MINERAL SUNSCREEN SPF 30- zinc oxide lotion
- NDC Code(s): 71585-136-00
- Packager: Salt and Stone LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 28, 2023
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- 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 a 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
Water, Cocos Nucifera (Coconut) Oil, Butyloctyl Salicylate, Diheptyl Succinate, Methyl Dihydroabietate, Butyrospermum Parkii (Shea Butter), Capryloyl Glycerin/Sebacic Acid Copolymer, Lavandula Angustifolia (Lavender) Oil, Theobroma Cacao (Cocoa) Seed Butter, Sodium Hyaluronate, Helianthus Annuus (Sunflower) Seed Oil*, Salvia Officinalis (Sage) Oil, Glycerin*, Caprylhydroxamic Acid, Camellia Sinensis (Green Tea) Leaf Extract*, Calendula Officinalis (Calendula) Flower Extract*, Withania Somnifera Root Extract.*, Tocopherol, Bisabolol, Cetyl Alcohol, Sodium Gluconate, Citric Acid, Microcrystalline Cellulose, Cellulose Gum, Caprylyl Glycol, Cetearyl Alcohol, Coco-Glucoside, Sodium Stearoyl Glutamate, Arachidyl Alcohol, Arachidyl Glucoside, Behenyl Alcohol, Polyhydroxystearic Acid. *Organic Ingredient
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INGREDIENTS AND APPEARANCE
SALT AND STONE NATURAL MINERAL SUNSCREEN SPF 30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71585-136 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 196 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCONUT OIL (UNII: Q9L0O73W7L) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) SHEA BUTTER (UNII: K49155WL9Y) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) LAVENDER OIL (UNII: ZBP1YXW0H8) COCOA BUTTER (UNII: 512OYT1CRR) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SUNFLOWER OIL (UNII: 3W1JG795YI) SAGE OIL (UNII: U27K0H1H2O) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) WITHANIA SOMNIFERA ROOT (UNII: V038D626IF) TOCOPHEROL (UNII: R0ZB2556P8) LEVOMENOL (UNII: 24WE03BX2T) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM GLUCONATE (UNII: R6Q3791S76) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) COCO GLUCOSIDE (UNII: ICS790225B) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) DOCOSANOL (UNII: 9G1OE216XY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71585-136-00 88 mL in 1 TUBE; Type 0: Not a Combination Product 08/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2019 Labeler - Salt and Stone LLC (080683697)
