Label: REJUVASKIN MINERAL FACIAL SUNSCREEN SPF 32 SHEER lotion
- NDC Code(s): 84375-101-01
- Packager: Atlantic Medical Products , LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 5, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- WHEN USING
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DO NOT USE
-
INACTIVE INGREDIENT
Inactive Ingredients
Benzyl Alcohol
Butyloctyl Salicylate
Caprylic/Capric Triglyceride
Citric Acid
Coco-Caprylate
Dehydroacetic Acid
Glycerin
Glyceryl Stearate
Niacinamide
Panthenol
Polyhydroxystearic Acid
Sodium Phytate
Saccharide Isomerate
Sodium Stearoyl Glutamate
Sucrose palmitate-stearate
Sucrose Laurate
Tocopheryl Acetate
Water
Xanthan Gum
- PURPOSE
- INDICATIONS & USAGE
-
DOSAGE & ADMINISTRATION
Directions
- Apply liberally to face and neck 15 minutes before sun exposure
- use a water-resistant sunscreen if swimming or sweating
- reapply at leat every two hours
- Sun Protection measures Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad-spectrum SPF of 15 or higher and other sun protection measures including
- limit time in the sun, especially from 10 am- 2 pm
- wear long-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a physician
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
REJUVASKIN MINERAL FACIAL SUNSCREEN SPF 32 SHEER
rejuvaskin mineral facial sunscreen spf 32 sheer lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84375-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20 g in 100 g Inactive Ingredients Ingredient Name Strength DEHYDROACETIC ACID (UNII: 2KAG279R6R) NIACINAMIDE (UNII: 25X51I8RD4) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) COCO-CAPRYLATE (UNII: 4828G836N6) SUCROSE STEARATE (UNII: 274KW0O50M) XANTHAN GUM (UNII: TTV12P4NEE) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) PANTHENOL (UNII: WV9CM0O67Z) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) PHYTATE SODIUM (UNII: 88496G1ERL) SACCHARIDE ISOMERATE (UNII: W8K377W98I) GLYCERIN (UNII: PDC6A3C0OX) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) SUCROSE STEARATE/PALMITATE ESTER (75% MONO ESTER) (UNII: L98X941W2B) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SUCROSE LAURATE (UNII: 05Q7CD0E49) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84375-101-01 60 g in 1 TUBE; Type 0: Not a Combination Product 06/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 06/04/2024 Labeler - Atlantic Medical Products , LLC (014302733) Establishment Name Address ID/FEI Business Operations Inspec Solutions 081030372 manufacture(84375-101)
