Label: PROTECTIVE DAY- avobenzone, homosalate, octinoxate, octocrylene cream
- NDC Code(s): 51861-090-00
- Packager: USANA Health Sciences, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Purpose
- Uses
- Warnings
- (continued) Drug Facts
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Directions:
• Apply 2-3 pumps of product 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.–2:00 p.m.• wear long-sleeved shirts, pants, hats, and sunglasses Sun Protection Measures
• Children under 6 months of age: Ask a doctor
- (continued) Drug Facts
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Inactive Ingredients:
Water, Butylene Glycol, Tribehenin PEG-20 Esters, Isopropyl Lauroyl Sarcosinate, Pentylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isodecyl Neopentanoate, Cyclopentasiloxane, Ocimum Basilicum Hairy Root Culture Extract, Citrullus Lanatus (Watermelon) Fruit Extract, Olea Europaea (Olive) Fruit Extract*, Lens Esculenta (Lentil) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Glycine Soja (Soybean) Seed Extract, Acanthopanax Senticosus (Eleuthero) Root Extract, Panax Ginseng Root Extract, Panax Quinquefolius Root Extract, Butyrospermum Parkii (Shea) Butter, Ceramide NP, Rosa Multiflora Fruit Extract, Potassium Hydroxide, Sodium Lactate, Salicornia Herbacea Extract, Hydrolyzed Corn Starch, Sodium PCA, Diisopropyl Sebacate, Lauryl Lactate, Caprylic/Capric Triglyceride, Glycerin, Silica, Citric Acid, Fragrance.
- Other Information
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INGREDIENTS AND APPEARANCE
PROTECTIVE DAY
avobenzone, homosalate, octinoxate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51861-090 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 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TRIBEHENIN PEG-20 ESTERS (UNII: 84K9EH29Y9) ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J) PENTYLENE GLYCOL (UNII: 50C1307PZG) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) ISODECYL NEOPENTANOATE (UNII: W60VYE24XC) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) OCIMUM BASILICUM ROOT (UNII: 0ZW1H84PHV) WATERMELON (UNII: 231473QB6R) BLACK OLIVE (UNII: 2M6QWV94OC) VICIA LENS FRUIT (UNII: ZYZ076G9JH) APPLE (UNII: B423VGH5S9) SOYBEAN (UNII: L7HT8F1ZOD) ELEUTHERO (UNII: ZQH6VH092Z) ASIAN GINSENG (UNII: CUQ3A77YXI) AMERICAN GINSENG (UNII: 8W75VCV53Q) SHEA BUTTER (UNII: K49155WL9Y) CERAMIDE NP (UNII: 4370DF050B) ROSA MULTIFLORA FRUIT (UNII: EZ5DSL4T27) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) SODIUM LACTATE (UNII: TU7HW0W0QT) SALICORNIA EUROPAEA WHOLE (UNII: 6ADL50JAKW) STARCH, CORN (UNII: O8232NY3SJ) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) LAURYL LACTATE (UNII: G5SU0BFK7O) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51861-090-00 1 in 1 CARTON 08/20/2024 1 28 g 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 08/20/2024 Labeler - USANA Health Sciences, Inc. (804413250) Registrant - USANA Health Sciences, Inc. (804413250) Establishment Name Address ID/FEI Business Operations Universal Packaging Systems, Inc. (DBA Paklab) 177711082 manufacture(51861-090)
