Label: OIL-FREE DAILY HYDRATION SPF 15- octinoxate, avobenzone cream
- NDC Code(s): 76151-105-11, 76151-105-52
- Packager: Boscia LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- Use
- WARNINGS
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- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Butylene Glycol, Silica, Glycerin, Polyglyceryl-10 Stearate, Pentylene Glycol, Simmondsia Chinensis (Jojoba) Leaf Extract, Epilobium Angustifolium Flower/leaf/stem Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Algae Extract, Hydrolyzed Yeast Extract, Arctium Lappa Root Extract, Phellodendron Amurense Bark Extract, Hydrogenated Rapeseed Alcohol, Hydroxyethylcellulose, Sclerotium Gum, Aluminum Hydroxide, Potassium Phosphate, Citrus Aurantium Amara (Bitter Orange) Flower Extract, Zinc Oxide, Titanium Dioxide.
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DESCRIPTION
Preservative-free. Dermatologist tested. Non-comedogenic. Alcohol-free, pH balanced, 100% natural fragrance and color, no animals testing and no animal ingredients. An oil-free moisturizer that hydrates the skin, minimizes pores and providers broad spectrum SPF 15. Polysaccharide provides essential moisture, silica powder controls excessive oil while wine Yeast and Marine Complex help protect against external elements. www.boscia.net B105-11 Distributed by boscia LLC. Irvine, CA 92614 Made in Japan U8-2
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INGREDIENTS AND APPEARANCE
OIL-FREE DAILY HYDRATION SPF 15
octinoxate, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76151-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) GLYCERIN (UNII: PDC6A3C0OX) PENTYLENE GLYCOL (UNII: 50C1307PZG) EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D) ROSEMARY (UNII: IJ67X351P9) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G) HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) POTASSIUM PHOSPHATE (UNII: B7862WZ632) CITRUS AURANTIUM FLOWER (UNII: O730ZX2Z83) ZINC OXIDE (UNII: SOI2LOH54Z) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76151-105-52 15 mL in 1 TUBE; Type 0: Not a Combination Product 12/19/2017 2 NDC:76151-105-11 40 mL in 1 TUBE; Type 0: Not a Combination Product 12/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/16/2011 Labeler - Boscia LLC (967960951) Establishment Name Address ID/FEI Business Operations Englewood Lab, Inc. 172198223 manufacture(76151-105)