Label: KINFIELD DAILY DEW SEA KELP MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 35- kinfield daily dew sea kelp moisturizer sunscreen lotion broad spectrum spf 35 lotion
- NDC Code(s): 81750-010-60
- Packager: Kinfield, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 January 10, 2023
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- Active Ingredients
- Uses
- Warnings
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Directions
• apply generously 15 minutes before sun exposure
• reapply: •after 40 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-sleeved shirts, pants, hats, and sunglasses
• children under 6 months of age: Ask a doctor -
Inactive ingredients
Water, Capylyl Caprylate/Caprate, Glycerin, Coco-Caprylate, Capric/Caprylic Triglyceride, Polyglycerl-2-Oleate, Polyhydroxystearic Acid, Polyglycerl-2 Stearate, Magnesium Sulfate, Hydrogenated Methyl Abietate, Galactoarabinan, Capryloyl Glycerin/Sebacic Acid Copolymer, Diheptyl Succinate, Cocos Nucifera (Coconut) Oil, Glyceryl Caprylate, Laminaria Digitata Extract, Triethoxycaprylylsilane, Propanediol, Caprylhydroxamic Acid, Aloe Barbadensis Leaf Extract, Oryza Sativa Bran Extract, Rosmarinus Officinalis Extract, Helianthus Annuus Seed Extract, Tocopherol, Natural Fragrance
- Other Information
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INGREDIENTS AND APPEARANCE
KINFIELD DAILY DEW SEA KELP MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 35
kinfield daily dew sea kelp moisturizer sunscreen lotion broad spectrum spf 35 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81750-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 20 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A) LAMINARIA DIGITATA (UNII: 15E7C67EE8) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) PROPANEDIOL (UNII: 5965N8W85T) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR) GLYCERIN (UNII: PDC6A3C0OX) COCO-CAPRYLATE (UNII: 4828G836N6) CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES (UNII: U72Q2I8C85) POLYGLYCERYL-2 OLEATE (UNII: 5759J47SAM) POLYGLYCERYL-2 STEARATE (UNII: 253MC0P0YV) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I) HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O) GALACTOARABINAN (UNII: SL4SX1O487) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) COCOS NUCIFERA WHOLE (UNII: 245J88W96L) ORYZA SATIVA WHOLE (UNII: 84IVV0906Z) ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) HELIANTHUS ANNUUS WHOLE (UNII: 17S27ZT6KR) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81750-010-60 1 in 1 PACKAGE 04/05/2021 1 60 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/05/2021 Labeler - Kinfield, Inc. (049511853)
