Label: EIGHT SAINTS CHASE THE SUN SPF-30- octocrylene, octisalate, zinc oxide cream
- NDC Code(s): 82247-384-00
- Packager: BRICKELL BRANDS 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 well 15-minuets before sun exposure • Reapply atleast every two hours. Immediately after drying swimming, or sweating. Spending time in the sun increases your risk of cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: - Limit time in sun between 10am–2pm. - Wear long sleeve shirts, pants, hats and sunglasses. - For children under 6-months, consult a physician. SUN PROTECTION MEASURES:
- Other Information:
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Other Ingredients:
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Camellia Sinensis (Green Tea) Extract, Caprylic/- Capric Triglyceride, Citric Acid, Cyclopentasiloxane, Cyclotetrasiloxane, Dacus Carota Sativa (Carrot) Extract, Citrullus Lanatus (Watermelon) Extract, Decyl Glucoside, Dimethicone, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Sunflower) Oil, Hyaluronic Acid, C13-14 Isoparaffin, Laureth-7, Lavandula Angustifolia (Lavender) Oil, Phenoxyethanol, Polyacrylamide, Punica Granatum (Pomegranate) Extract, Sclerocarya Birrea (Marula) Oil, Squalane, Tocopheryl Acetate (Vitamin E), Tridecyl Salicylate.
- Package Labeling:
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INGREDIENTS AND APPEARANCE
EIGHT SAINTS CHASE THE SUN SPF-30
octocrylene, octisalate, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82247-384 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) GREEN TEA LEAF (UNII: W2ZU1RY8B0) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 4 (UNII: CZ227117JE) CARROT (UNII: L56Z1JK48B) WATERMELON (UNII: 231473QB6R) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) DIMETHICONE (UNII: 92RU3N3Y1O) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) HYALURONIC ACID (UNII: S270N0TRQY) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) LAVENDER OIL (UNII: ZBP1YXW0H8) PHENOXYETHANOL (UNII: HIE492ZZ3T) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) SQUALANE (UNII: GW89575KF9) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82247-384-00 1 in 1 BOX 02/14/2022 1 59 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/14/2022 Labeler - BRICKELL BRANDS LLC (081141606)