Label: KINFIELD SUNGLOW LUMINIZING SUNSCREEN SPF 30 lotion
- NDC Code(s): 81750-030-60
- 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
-
Directions
• apply generously 15 minutes before sun exposure
• use a water-resistant sunscreen if swimming or sweating
• reapply 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, Coco-Caprylate, Dicaprylyl Carbonate, Cetyl
Alcohol, Microcrystalline Cellulose, Lauryl Glucoside,
Propanediol, Polyglyceryl-2 Dipolyhydroxystearate,
Phytic Acid, Cellulose Gum, Xanthan Gum, Triethoxycaprylylsilane,
Polyhydroxystearic Acid, Glycerin, Capryloyl
Glycerin/Sebacic Acid Copolymer, Diheptyl Succinate,
Helianthus Annuus (Sunflower) Seed Oil, Simmondsia
Chinensis (Jojoba) Seed Oil, Rosmarinus Officinalis
(Rosemary) Leaf Extract, Glyceryl Stearate
Citrate, Glyceryl Stearate, Caprylyl Glyceryl Ether, Caprylhydroxamic
Acid, Mica CI77019, Iron Oxides
CI77491, Titanium Dioxide CI77891, Natural Fragrance - Other Information
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INGREDIENTS AND APPEARANCE
KINFIELD SUNGLOW LUMINIZING SUNSCREEN SPF 30
kinfield sunglow luminizing sunscreen spf 30 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81750-030 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 20.3 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCO-CAPRYLATE (UNII: 4828G836N6) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) CETYL ALCOHOL (UNII: 936JST6JCN) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) PROPANEDIOL (UNII: 5965N8W85T) POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12) XANTHAN GUM (UNII: TTV12P4NEE) GLYCERIN (UNII: PDC6A3C0OX) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T) DIHEPTYL SUCCINATE (UNII: 057N7SS26Y) HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) SIMMONDSIA CHINENSIS LEAF (UNII: 67G221EK95) ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W) MICA (UNII: V8A1AW0880) BROWN IRON OXIDE (UNII: 1N032N7MFO) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81750-030-60 1 in 1 PACKAGE 06/14/2021 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)
