FDA.reportPublic FDA data

Sun Zapper - Pure Zinc Anti Mozzie Sunscreen SPF50

Manufacturer
VEGANIC SKN LIMITED
Effective date
2026-07-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-28 05:10:12

Label at a glance#

ProductSun Zapper - Pure Zinc Anti Mozzie 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

Please kindy refer to label

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 please

INACTIVE INGREDIENT SECTION

Please kindly refer to artwork

artworks

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label - 100gLabel - 100g

label 100g

Label - 240gLabel - 240g

artowrk 240g

previous label for 100gprevious label for 100g

previous label for 100g

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-139327694001351GTIN-13: 9327694001351
EAN-13: 9327694001351
GTIN storage (14 digits): 09327694001351		Sun Zapper Pure ZInc Anti mozzie - 100g.jpg

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83252-12283252-122-25, 83252-122-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
WATER059QF0KO0RIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ISOSTEARIC ACIDX33R8U0062IACT
CANDELILLA WAXWL0328HX19IACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCERINPDC6A3C0OXIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
XANTHAN GUMTTV12P4NEEIACT
FERRIC OXIDE RED1K09F3G675IACT
SODIUM HINOKITIOL5MPS47D679IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
POLYGLYCERYL-4 OLEATE15B05TY4GXIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
CITRONELLA OILQYO8Q067D0IACT
COCONUT ALKANES1E5KJY107TIACT
VANILLINCHI530446XIACT

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
Sun Zapper - Pure Zinc Anti Mozzie Sunscreen SPF50ZINC OXIDE SUNSCREENVEGANIC SKN LIMITED3cd83dba-2008-bef6-e063-6294a90aad952026-07-23WarningsExact identifier
ndc (package): 83252-122-25
ndc (package): 83252-122-17
ndc (product): 83252-122
ndc11 (package): 83252012217
ndc11 (package): 83252012225
spl id: 5752a007-5cab-6909-e063-6394a90a00e0
spl set id: 3cd83dba-2008-bef6-e063-6294a90aad95

Reported adverse events (FAERS/openFDA)#

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