Label: BABO BOTANICALS SENSITIVE BABY MINERAL SUNSCREEN SPF50- zinc oxide lotion
- NDC Code(s): 79265-8758-1
- Packager: Babo Botanicals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 30, 2025
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- Drug Facts
- Active ingredient
- Purpose
- 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.
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, Cocos Nucifera (Coconut) Oil, Butyloctyl Salicylate, Carthamus Tinctorius (Safflower) Seed Oil, Methyl Dihydroabietate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Sodium Stearoyl Glutamate, Microcrystalline Cellulose, Calendula Officinalis Flower Extract*, Chamomilla Recutita (Matricaria) Flower Extract*, Nasturtium Officinale (Watercress) Flower/Leaf Extract*, Spiraea Ulmaria (Meadowsweet) Flower Extract*, Theobroma Cacao (Cocoa) Seed Butter*, Bisabolol*, Tocopherol, Cetyl Alcohol, Caprylyl Glycol, Coco-Glucoside, Behenyl Alcohol, Arachidyl Glucoside, Arachidyl Alcohol, Polyhydroxystearic Acid, Citric Acid, Sodium Gluconate, Sodium Hyaluronate, Glycerin, Caprylhydroxamic Acid, Cellulose Gum..*Certified Organic Ingredients
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INGREDIENTS AND APPEARANCE
BABO BOTANICALS SENSITIVE BABY MINERAL SUNSCREEN SPF50
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79265-8758 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 200 mg in 1 mL Inactive Ingredients Ingredient Name Strength CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) TOCOPHEROL (UNII: R0ZB2556P8) LEVOMENOL (UNII: 24WE03BX2T) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) NASTURTIUM OFFICINALE FLOWERING TOP (UNII: W1N2U8I64G) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) SODIUM GLUCONATE (UNII: R6Q3791S76) CETYL ALCOHOL (UNII: 936JST6JCN) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311) CHAMOMILE (UNII: FGL3685T2X) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) DOCOSANOL (UNII: 9G1OE216XY) SHEA BUTTER (UNII: K49155WL9Y) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F) COCO GLUCOSIDE (UNII: ICS790225B) COCONUT OIL (UNII: Q9L0O73W7L) SUNFLOWER OIL (UNII: 3W1JG795YI) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) FILIPENDULA ULMARIA FLOWER (UNII: 06L18L32G6) COCOA BUTTER (UNII: 512OYT1CRR) SAFFLOWER OIL (UNII: 65UEH262IS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79265-8758-1 89 mL in 1 TUBE; 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)
