FDA.reportPublic FDA data

Sun Zapper - Kids pure zinc sunscreen SPF50

Manufacturer
VEGANIC SKN LIMITED
Effective date
2026-08-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-09 01:01:10

Label at a glance#

ProductSun Zapper - Kids pure zinc sunscreen SPF50
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc oxide - 25%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

kindly refer to label picture

WARNINGS SECTION

For external use only.

Do not use on damaged r broken skin.

When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Kindly refer to Label

INACTIVE INGREDIENT SECTION

See ingredients on label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label - 100gLabel - 100g

Artwork

Tube:

Tube artworkTube artwork

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-139327694001399GTIN-13: 9327694001399
EAN-13: 9327694001399
GTIN storage (14 digits): 09327694001399		Sun Zapper Kids.jpg

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83252-12383252-123-25, 83252-123-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCERINPDC6A3C0OXIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
XANTHAN GUMTTV12P4NEEIACT
FERRIC OXIDE RED1K09F3G675IACT
SODIUM HINOKITIOL5MPS47D679IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
COCONUT ALKANES1E5KJY107TIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ISOSTEARIC ACIDX33R8U0062IACT
CANDELILLA WAXWL0328HX19IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-03-08full-release2026-06-01 01:49:17

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
4c8c9a92-4aed-503a-e063-6394a90a3b503ee4410b-46d8-1059-e063-6394a90a7f962026-03-08WarningsExact identifier
spl set id: 3ee4410b-46d8-1059-e063-6394a90a7f96

Reported adverse events (FAERS/openFDA)#

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