Label: BABO BOTANICALS SHEER ZINC MINERAL SUNSCREEN SPF30- zinc oxide spray
- NDC Code(s): 79265-7908-1
- Packager: Babo Botanicals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 30, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- Shake well
- Hold container 4 to 6 inches from the skin to apply
- Apply liberally 15 minutes before sun exposure
- Do not spray directly into face
- Spray into hands and then apply to 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 sleeve shirts, pants, hats, and sunglasses
- Children under 6 months: Ask a doctor.
- Other information
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Inactive ingredients
Water (Aqua), Butyloctyl Salicylate, Bentonite, Carthamus Tinctorius (Safflower) Seed Oil, Heptyl Undecylenate, Methyl Dihydroabietate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Jojoba Esters, Helianthus Annuus (Sunflower) Seed Oil*, Calendula Officinalis Flower Extract*, Chamomilla Recutita (Matricaria) Flower Extract*, Nasturtium Officinale (Watercress) Flower/Leaf Extract*, Spiraea Ulmaria (Meadowsweet) Flower Extract*, Glycerin, Coco-Glucoside, Caprylyl Glycol, Caprylhydroxamic Acid, Cetearyl Alcohol.
*Certified Organic Ingredients
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INGREDIENTS AND APPEARANCE
BABO BOTANICALS SHEER ZINC MINERAL SUNSCREEN SPF30
zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79265-7908 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 120 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CHAMOMILE (UNII: FGL3685T2X) SUNFLOWER OIL (UNII: 3W1JG795YI) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6) BENTONITE (UNII: A3N5ZCN45C) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) CAPRYLYL GLYCOL (UNII: 00YIU5438U) WATER (UNII: 059QF0KO0R) SAFFLOWER OIL (UNII: 65UEH262IS) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) NASTURTIUM OFFICINALE FLOWERING TOP (UNII: W1N2U8I64G) COCO GLUCOSIDE (UNII: ICS790225B) HEPTYL UNDECYLENATE (UNII: W77QUB6GXO) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79265-7908-1 177 mL in 1 CAN; Type 0: Not a Combination Product 10/30/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/30/2023 Labeler - Babo Botanicals, Inc. (058258734)
