Label: MUSTELA MINERAL SUNSCREEN BROAD SPECTRUM SPF 50- zinc oxide, titanium dioxide spray
- NDC Code(s): 64768-2927-1
- Packager: Expanscience Laboratories d/b/a Mustela
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 23, 2023
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- Drug Facts
- Active ingredients
- Purpose
- Uses
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Warnings
- Do not store at temperature above 120F.
- Contents under pressure. Do not puncture or incinerate can.
- Avoid using on children under 3
- For external use only. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal
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Directions
- Shake well before use
- Hold container 4 to 6 inches from the skin to apply
- Apply liberally 15 minutes before sun exposure
- Do not spray directly into face
- Do not spray in windy condition
- Use in well-ventilated area
- 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 risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other protection measures including:
- Limit time in the sun, especially from 10 a.m - 2p.m
- Wear long-sleeved shirt, pants, hat, and sunglasses
- Children under 6 months: ask a doctor.
- Other information
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Inactive ingredients
Water, Helianthus Annuus (Sunflower) Seed Oil, Olea Europaea (Olive) Fruit Oil, Butyloctyl Salicylate, Cocos Nucifera (Coconut) Oil, Capryloyl Glycerin/Sebacic Acid Copolymer, Heptyl Undecylenate, Methyl Dihydroabietate, Cetearyl Alcohol, Propanediol, Sodium Stearoyl Glutamate, Bentonite, Tocopherol, Caprylyl Glycol, Coco-Glucoside, Microcrystalline Cellulose, Bisabolol*, Alumina, Polyhydroxystearic Acid, Citric Acid, Sodium Gluconate, Caprylhydroxamic Acid, Glycerin, Silica, Cellulose Gum, Aloe Barbadensis Leaf Juice*, Calendula Officinalis Flower Extract*, Chamomilla Recutita (Matricaria) Flower Extract*, Spiraea Ulmaria Flower Extract*, Nasturtium Officinale Flower/Leaf Extract*, *Certified Organic Ingredients
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INGREDIENTS AND APPEARANCE
MUSTELA MINERAL SUNSCREEN BROAD SPECTRUM SPF 50
zinc oxide, titanium dioxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64768-2927 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 147 mg in 1 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 43 mg in 1 g Inactive Ingredients Ingredient Name Strength HEPTYL UNDECYLENATE (UNII: W77QUB6GXO) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) BENTONITE (UNII: A3N5ZCN45C) CAPRYLYL GLYCOL (UNII: 00YIU5438U) COCO GLUCOSIDE (UNII: ICS790225B) ALUMINUM OXIDE (UNII: LMI26O6933) SODIUM GLUCONATE (UNII: R6Q3791S76) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CHAMOMILE (UNII: FGL3685T2X) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) LEVOMENOL (UNII: 24WE03BX2T) NASTURTIUM OFFICINALE FLOWERING TOP (UNII: W1N2U8I64G) SUNFLOWER OIL (UNII: 3W1JG795YI) FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) OLIVE OIL (UNII: 6UYK2W1W1E) COCONUT OIL (UNII: Q9L0O73W7L) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPANEDIOL (UNII: 5965N8W85T) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64768-2927-1 170 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 05/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2021 Labeler - Expanscience Laboratories d/b/a Mustela (181191057)