Label: BABO BOTANICALS SENSITIVE BABY MINERAL SUNSCREEN SPF30- zinc oxide spray
- NDC Code(s): 79265-9758-1
- Packager: Babo Botanicals, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 26, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- Shake well
- Apply liberally 15 minutes before sun exposure.
- 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. – 2 p.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), Helianthus Annuus (Sunflower) Seed Oil*, Butyloctyl Salicylate, Tetradecane, Caprylic/Capric Triglyceride, Carthamus Tinctorius (Safflower) Seed Oil, Methyl Dihydroabietate, Bentonite, Cetearyl Alcohol, Propanediol, Calendula Officinalis Flower Extract*, Chamomilla Recutita (Matricaria) Flower Extract*, Nasturtium Officinale Flower/Leaf Extract*, Spiraea Ulmaria Flower Extract*, Glycerin, Jojoba Esters, Bisabolol*, Tocopherol, Caprylyl Glycol, Microcrystalline Cellulose, Coco-Glucoside, Polyhydroxystearic Acid, Caprylhydroxamic Acid, Cellulose Gum.
*Certified Organic Ingredients
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INGREDIENTS AND APPEARANCE
BABO BOTANICALS SENSITIVE BABY MINERAL SUNSCREEN SPF30
zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79265-9758 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 145 mg in 1 mL Inactive Ingredients Ingredient Name Strength TETRADECANE (UNII: 03LY784Y58) WATER (UNII: 059QF0KO0R) BENTONITE (UNII: A3N5ZCN45C) CAPRYLYL GLYCOL (UNII: 00YIU5438U) LEVOMENOL (UNII: 24WE03BX2T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CHAMOMILE (UNII: FGL3685T2X) GLYCERIN (UNII: PDC6A3C0OX) SUNFLOWER OIL (UNII: 3W1JG795YI) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) PROPANEDIOL (UNII: 5965N8W85T) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) SAFFLOWER OIL (UNII: 65UEH262IS) COCO GLUCOSIDE (UNII: ICS790225B) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) NASTURTIUM OFFICINALE FLOWERING TOP (UNII: W1N2U8I64G) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79265-9758-1 177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 10/26/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/26/2023 Labeler - Babo Botanicals, Inc. (058258734)