Label: EUCERIN SENSITIVE MINERAL SPF 50 SUNSCREEN- zinc oxide lotion
- NDC Code(s): 66800-1000-1, 66800-1000-2
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 3, 2023
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- Drug Facts
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
■ apply liberally 15 minutes before sun exposure
■ reapply:
■ after 80 minutes of swimming or sweating
■ immediately after towel drying
■ at least every 2 hours
■ Sun Protection Measures. 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-sleeve shirts, pants, hats, and sunglasses
■ children under 6 months: Ask a doctor
- Other information
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Inactive ingredients
Water, C12-15 Alkyl Benzoate, Isopropyl Palmitate, Butyloctyl Salicylate, Ethylhexyl Pelargonate, Cetyl PEG/PPG-10/1 Dimethicone, Propylene Glycol, Cyclopentasiloxane, Bis-Octyldodecyl Dimer Dilinoleate/Propanediol Copolymer, Dimethicone, Ethylhexyl Methoxycrylene, Polyester-27, Triethoxycaprylylsilane, Beeswax, Hydroxyacetophenone, Sodium Chloride, PEG-12 Dimethicone Crosspolymer, 1,2-Hexanediol, Caprylyl Glycol, Tocopherol
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INGREDIENTS AND APPEARANCE
EUCERIN SENSITIVE MINERAL SPF 50 SUNSCREEN
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66800-1000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 24 g in 100 g Inactive Ingredients Ingredient Name Strength ETHYLHEXYL PELARGONATE (UNII: 3YU1SQ04DV) CAPRYLYL GLYCOL (UNII: 00YIU5438U) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) TOCOPHEROL (UNII: R0ZB2556P8) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) POLYESTER-7 (UNII: 0841698D2F) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) HYDROXYACETOPHENONE (UNII: G1L3HT4CMH) SODIUM CHLORIDE (UNII: 451W47IQ8X) BIS-OCTYLDODECYL DIMER DILINOLEATE/PROPANEDIOL COPOLYMER (UNII: TY3J98ZR7R) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) Product Characteristics Color white (off-white to yellow) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66800-1000-1 118 g in 1 TUBE; Type 0: Not a Combination Product 11/03/2021 2 NDC:66800-1000-2 14 g in 1 POUCH; Type 0: Not a Combination Product 03/03/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 11/03/2021 Labeler - Beiersdorf Inc (001177906)
