FDA.reportPublic FDA data

Kinfield Sunglow Luminizing Sunscreen SPF 30

Manufacturer
Kinfield, Inc.
Effective date
2024-12-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:44:39

Label at a glance#

ProductKinfield Sunglow Luminizing Sunscreen SPF 30
Active ingredientZINC OXIDE
Label structure10 sections

Indications and uses

• helps prevent sunburn • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Dosage and administration

• 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, ...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 20.3%

Uses

INDICATIONS & USAGE SECTION

• helps prevent sunburn • if used as directed with other
sun protection measures (see Directions), decreases the
risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a docor if rash occurs

Keep out of reach of children. If swalled, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

• protect the product in this container from excessive
heat and direct sun

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Purpose

OTC - PURPOSE SECTION

Purpose: Sunscreen

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

81750-030-6081750-030-60

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81750-030-602024-07-30C16284748780-11030e365-657c-111a-e063-dadaa90a10e2DRUG FACTS
81750-030-602024-01-30C16284748780-11030e365-657c-111a-e063-dadaa90a10e2DRUG FACTS

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81750-030KINFIELD SUNGLOW LUMINIZING SUNSCREEN SPF 30 LOTION [KINFIELD, INC.]5Legacy NDC20241222_346409ee-ae61-463c-aea3-048b82cd9927.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81750-03081750-030-60

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCO-CAPRYLATE4828G836N6IACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
CETYL ALCOHOL936JST6JCNIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
PROPANEDIOL5965N8W85TIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
DIHEPTYL SUCCINATE057N7SS26YIACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
SIMMONDSIA CHINENSIS LEAF67G221EK95IACT
ROSMARINUS OFFICINALIS FLOWERNR1A27F29OIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
MICAV8A1AW0880IACT
BROWN IRON OXIDE1N032N7MFOIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
ZINC OXIDESOI2LOH54ZACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4526b3c8-7afe-f466-e063-6394a90a109a346409ee-ae61-463c-aea3-048b82cd99272025-12-04WarningsExact identifier
spl set id: 346409ee-ae61-463c-aea3-048b82cd9927

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.