Label: USANA CELAVIVE DAILY MINERAL PROTECTIVE CREAM MOISTURIZER WITH SUNSCREEN SPF 30- zinc oxide cream
- NDC Code(s): 51861-080-00
- Packager: USANA Health Sciences, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions:
- Apply to forehead, cheeks, nose, chin, and neck as the last step in your daytime skincare routine.
- Apply generously and evenly 15 minutes before sun exposure.
- Reapply at least every 2 hours.
- Use a water-resistant sunscreen if swimming or sweating.
- 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.
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: Sun Protection Measures:
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Inactive Ingredients:
Water, C13-15 Alkane, Propanediol, C15-19 Alkane, Caprylic/Capric Triglyceride, Pentylene Glycol, Polyhydroxystearic Acid, Isostearic Acid, Lecithin, Polyglyceryl-3 Polyricinoleate, Maltodextrin, Bis-Diglyceryl Polyacyladipate-2, Gluconolactone, Polyacrylate Crosspolymer-6, Inositol, Silica, Arachidyl Alcohol, Polyglycerin-3, Polyglyceryl-3 Lactate/Laurate, Sodium Benzoate, Tocopherol, Bisabolol, Cetearyl Alcohol, Coco- Glucoside, Glucose, Xanthan Gum, Behenyl Alcohol, Sodium Citrate, Sodium Dilauramidoglutamide Lysine, Sclerotium Gum, Fragrance, Arachidyl Glucoside, Citric Acid, Caesalpinia Spinosa Gum, Sodium Phytate, Physalis Alkekengi Calyx Extract, T-Butyl Alcohol, Calcium Gluconate, Helianthus Annuus Sprout Extract, Limonene, Beta-Carotene.
- Other Information
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INGREDIENTS AND APPEARANCE
USANA CELAVIVE DAILY MINERAL PROTECTIVE CREAM MOISTURIZER WITH SUNSCREEN SPF 30
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51861-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 182 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM DILAURAMIDOGLUTAMIDE LYSINE (UNII: MNJ7VPT2R5) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) WATER (UNII: 059QF0KO0R) C13-15 ALKANE (UNII: 114P5I43UJ) PROPANEDIOL (UNII: 5965N8W85T) C15-19 ALKANE (UNII: CI87N1IM01) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PENTYLENE GLYCOL (UNII: 50C1307PZG) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ISOSTEARIC ACID (UNII: X33R8U0062) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) MALTODEXTRIN (UNII: 7CVR7L4A2D) BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T) GLUCONOLACTONE (UNII: WQ29KQ9POT) AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9) INOSITOL (UNII: 4L6452S749) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) POLYGLYCERYL-3 LAURATE (UNII: Y9ZSR39D0E) SODIUM BENZOATE (UNII: OJ245FE5EU) TOCOPHEROL (UNII: R0ZB2556P8) LEVOMENOL (UNII: 24WE03BX2T) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) COCO GLUCOSIDE (UNII: ICS790225B) ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) XANTHAN GUM (UNII: TTV12P4NEE) DOCOSANOL (UNII: 9G1OE216XY) SODIUM CITRATE (UNII: 1Q73Q2JULR) BETASIZOFIRAN (UNII: 2X51AD1X3T) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CAESALPINIA SPINOSA RESIN (UNII: WL3883U2PO) PHYTATE SODIUM (UNII: 88496G1ERL) PHYSALIS ALKEKENGI CALYX (UNII: AL7F9NO9HR) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) CALCIUM GLUCONATE (UNII: SQE6VB453K) HELIANTHUS ANNUUS SPROUT (UNII: 4P26HG1S5W) LIMONENE, (+)- (UNII: GFD7C86Q1W) BETA CAROTENE (UNII: 01YAE03M7J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51861-080-00 1 in 1 CARTON 04/09/2021 1 50 mL in 1 BOTTLE, PLASTIC; 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 04/09/2021 Labeler - USANA Health Sciences, Inc. (804413250)
