Label: BRO GLO SUNSCREEN FOR THE BOYS SPF30 lotion
- NDC Code(s): 84222-001-01
- Packager: Foshan Miwei Cosmetics Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 2, 2024
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- Official Label (Printer Friendly)
- PURPOSE
- ACTIVE INGREDIENT
- WHEN USING
- WARNINGS
- DO NOT USE
- INDICATIONS & USAGE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
*Apply generously and evenly 15 minutes before sun exposure
*Reapply after 40 minutes of swimming or sweating
Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with a broad spectrum SPF value of 15 or higher and other sun protection measures including:
*Limit time in the sun, especially from 10 am.-2 pm.
*Wear long-sleeve shirts, pants, hats, and sunglasses Children under 6 months of age : Ask a doctor
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Organic Aloe Barbadensis (Aloe Vera) Leaf Juice, Organic Cocos Nucifera (Coconut) Oil, Organic Butyrospermum Parkii (Shea Butter), Glycerin (Vegetable), Sorbitan Sesquioleate, Ricinus Communis (Castor) Seed Oil, Organic Helianthus Annuus (Sunflower) Oil, Organic Beeswax, Polyhydroxystearic Acid, Organic Cucumis Sativus (Cucumber) Fruit Extract, Organic Calendula Officinalis (Calendula) Flower Extract, Organic Vanilla Planifolia (Vanilla) Fruit Extract, Organic Camellia Oleifera (Japanese Green Tea) Leaf Extract, Rosmarinus Officinalis Leaf Extract, Magnesium Sulfate, Tocopherol (Vitamin E), Cocos Nucifera (Coconut) Pulp Extract, Vanilla Tahitensis (Vanilla) Fruit Extract, 1,2-Hexanediol and Hydroxyacetophenone.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BRO GLO SUNSCREEN FOR THE BOYS SPF30
bro glo sunscreen for the boys spf30 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84222-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 16 g in 100 mL Inactive Ingredients Ingredient Name Strength SHEA BUTTER (UNII: K49155WL9Y) 6.6 mL in 100 mL HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) 0.05 mL in 100 mL YELLOW WAX (UNII: 2ZA36H0S2V) 0.5 mL in 100 mL CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) 0.5 mL in 100 mL CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) 0.1 mL in 100 mL COCONUT (UNII: 3RT3536DHY) 0.1 mL in 100 mL ALOE VERA LEAF (UNII: ZY81Z83H0X) 50.6 mL in 100 mL CASTOR OIL (UNII: D5340Y2I9G) 3 mL in 100 mL 1,2-HEXANEDIOL (UNII: TR046Y3K1G) 0.05 mL in 100 mL MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB) 0.1 mL in 100 mL TOCOPHEROL (UNII: R0ZB2556P8) 0.1 mL in 100 mL POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) 0.5 mL in 100 mL CUCUMBER (UNII: YY7C30VXJT) 0.5 mL in 100 mL VANILLA BEAN (UNII: Q74T35078H) 0.1 mL in 100 mL ROSEMARY (UNII: IJ67X351P9) 0.1 mL in 100 mL GLYCERIN (UNII: PDC6A3C0OX) 6 mL in 100 mL TAHITIAN VANILLA BEAN (UNII: 0M3NVJ6AX3) 0.1 mL in 100 mL COCONUT OIL (UNII: Q9L0O73W7L) 10 mL in 100 mL SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) 3 mL in 100 mL SUNFLOWER OIL (UNII: 3W1JG795YI) 2 mL in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84222-001-01 100 mL in 1 TUBE; Type 0: Not a Combination Product 04/03/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/03/2024 Labeler - Foshan Miwei Cosmetics Co., Ltd. (554530932)
