Label: SUNNY Q BROAD SPECTRUM SPF-30- zinc oxide lotion
- NDC Code(s): 81738-138-00
- Packager: Sunny Q Sunscreen LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2023
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- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
• Apply liberally 15 minutes before sun exposure. • Children under 6 months of age: ask a doctor. • Reapply at least every 2 hours. • Reapply as needed or after towel drying, swimming, or sweating. • Use a water-resistant sunscreen if swimming or sweating. • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measures including: • Limit time in the sun, especially from 10 a.m. - 2 p.m. • Wear long-sleeved shirts, pants, hats, and sunglasses.
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Inactive Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Ascorbic Acid (Vitamin C), Butyrospermum Parkii (Shea) Butter, Camellia Sinensis (Green Tea) Extract, Cannabis Sativa (Hemp Seed) Oil, Citrullus Lanatus (Watermelon) Extract, Caprylic/Capric Triglyceride, Decyl Glucoside, Ethyl Vanillin, Glycerin, Glyceryl Caprylate, Glyceryl Stearate, Glyceryl Undecylenate, Helianthus Annuus (Sunflower) Oil, Hydroxyethylcellulose, Iron Oxides (Black, Red, White, Yellow), Mangifera Indica (Mango) Butter, Persea Gratissima (Avacado) Oil, Polyhydroxystearic Acid, Prunus Amygdalus Dulcis (Almond) Oil, Rosmarinus Officinalis (Rosemary) Oil, Rubus Idaeus (Raspberry) Fruit Extract, Simmondsia Chinensis (Jojoba) Oil, Stearic Acid, Xanthan Gum, Zemea (Corn) Propanediol.
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INGREDIENTS AND APPEARANCE
SUNNY Q BROAD SPECTRUM SPF-30
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81738-138 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 200 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) ASCORBIC ACID (UNII: PQ6CK8PD0R) SHEA BUTTER (UNII: K49155WL9Y) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CANNABIS SATIVA SEED (UNII: QE567Z26NG) WATERMELON (UNII: 231473QB6R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) ETHYL VANILLIN (UNII: YC9ST449YJ) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) FERRIC OXIDE RED (UNII: 1K09F3G675) MANGO (UNII: I629I3NR86) AVOCADO OIL (UNII: 6VNO72PFC1) ALMOND (UNII: 3Z252A2K9G) ROSEMARY (UNII: IJ67X351P9) RASPBERRY (UNII: 4N14V5R27W) JOJOBA OIL (UNII: 724GKU717M) STEARIC ACID (UNII: 4ELV7Z65AP) XANTHAN GUM (UNII: TTV12P4NEE) CORN (UNII: 0N8672707O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81738-138-00 100.55 mL in 1 JAR; Type 0: Not a Combination Product 03/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 03/01/2021 Labeler - Sunny Q Sunscreen LLC (117886019)
