Label: PROTECTIVE DAY- avobenzone, homosalate, octinoxate, octocrylene lotion
- NDC Code(s): 51861-060-00
- Packager: USANA Health Sciences, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- Active Ingredients
- Purpose
- Uses
- Warnings
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DOSAGE & ADMINISTRATION
• Shake well and apply a pearl-sized amount to face and neck • Apply generously and evenly 15 minutes before sun exposure • Reapply at least every 2 hours • Use a water resistant sunscreen if swimming or sweating • . 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 value 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 • Children under 6 months of age: Ask a doctor
Sun Protection Measures -
Inactive Ingredients:
Water, Butylene Glycol, Isopropyl Lauroyl Sarcosinate, Pentylene Glycol, Mica, Ethylhexyl Palmitate, Cetearyl Alcohol, Dimethicone, Polysorbate 60, Ocimum Basilicum Hairy Root Culture Extract, Glycine Soja (Soybean) Seed Extract, Olea Europaea (Olive) Fruit Extract, Citrullus Lanatus (Watermelon) Fruit Extract, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Acanthopanax Senticosus (Eleuthero) Root Extract, Panax Ginseng Root Extract, Panax Quinquefolius Root Extract, Butyrospermum Parkii (Shea) Butter, Rosa Multiflora Fruit Extract, Ceramide NP, Sodium PCA,Glycerin, Sodium Lactate, Ceteth-10 Phosphate, Dicetyl Phosphate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Silica, Hydrolyzed Corn Starch, Citric Acid, Potassium Hydroxide, Fragrance.
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INGREDIENTS AND APPEARANCE
PROTECTIVE DAY
avobenzone, homosalate, octinoxate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51861-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J) PENTYLENE GLYCOL (UNII: 50C1307PZG) MICA (UNII: V8A1AW0880) ETHYLHEXYL PALMITATE (UNII: 2865993309) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) POLYSORBATE 60 (UNII: CAL22UVI4M) SOYBEAN (UNII: L7HT8F1ZOD) BLACK OLIVE (UNII: 2M6QWV94OC) WATERMELON (UNII: 231473QB6R) LENS CULINARIS FRUIT (UNII: ZYZ076G9JH) APPLE (UNII: B423VGH5S9) ELEUTHERO (UNII: ZQH6VH092Z) ASIAN GINSENG (UNII: CUQ3A77YXI) AMERICAN GINSENG (UNII: 8W75VCV53Q) SHEA BUTTER (UNII: K49155WL9Y) ROSA MULTIFLORA FRUIT (UNII: EZ5DSL4T27) CERAMIDE NP (UNII: 4370DF050B) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LACTATE (UNII: TU7HW0W0QT) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51861-060-00 1 in 1 CARTON 08/01/2017 1 30 mL in 1 BOTTLE; 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 08/01/2017 Labeler - USANA Health Sciences, Inc. (804413250)