FDA.reportPublic FDA data

Sparms 100% Organic Face Sunscreen

Manufacturer
VEGANIC SKN LIMITED
Effective date
2026-02-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:45:57

Label at a glance#

ProductSparms 100% Organic Face Sunscreen
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 - 70gLabel - 70g

Label - 1kgLabel - 1kg

Label - 2kgLabel - 2kg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-139337907073853GTIN-13: 9337907073853
EAN-13: 9337907073853
GTIN storage (14 digits): 09337907073853		Sparms Label 2kg.jpg
QR code linkQR Codewww.ebs.tga.gov.au/servlet/xmlmillr6?dbid=ebs/PublicHTML/pdfStore.nsf&docid=519486&agid=%28PrintDetailsPublic%29&actionid=1Sparms Label 1kg.jpg, Sparms Label 70g.jpg, Sparms Label 2kg.jpg
Data codeCode 1289351644008992Sparms Label 70g.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83252-143-01Sparms 100% Organic Face Sunscreen0.07 kg in 1 BOTTLE, PUMPCREAM0.071
83252-143-15Sparms 100% Organic Face Sunscreen2 kg in 1 BOTTLE, PUMPCREAM21
83252-143-21Sparms 100% Organic Face Sunscreen1 kg in 1 BOTTLE, PUMPCREAM11

Products#

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

DailyMed product names page 1 of 1 · 30 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83252-14383252-143-21, 83252-143-15, 83252-143-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
COCONUT ALKANES1E5KJY107TIACT
PELARGONIUM GRAVEOLENS FLOWER OIL3K0J1S7QGCIACT
POMEGRANATE56687D1Z4DIACT
GLYCERYL STEARATE CITRATEWH8T92A065IACT
SODIUM HYALURONATEYSE9PPT4THIACT
SODIUM CHLORIDE451W47IQ8XIACT
POLYGLYCERYL-3 RICINOLEATEMZQ63P0N0WIACT
SODIUM ASCORBATES033EH8359IACT
XANTHAN GUMTTV12P4NEEIACT
FERRIC OXIDE RED1K09F3G675IACT
BISABOLOL24WE03BX2TIACT
SODIUM HINOKITIOL5MPS47D679IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
CORIANDER OIL7626GC95E5IACT
KAKADU PLUM0ZQ1D2FDLIIACT
CITRUS PARADISI (GRAPEFRUIT) SEED OIL598D944HOLIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
BANANA4AJZ4765R9IACT
HIPPOPHAE RHAMNOIDES SEED OILT53SBG6741IACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
WATER059QF0KO0RIACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ISOSTEARIC ACIDX33R8U0062IACT
CANDELILLA WAXWL0328HX19IACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
MANDARIN OILNJO720F72RIACT
ZINC OXIDESOI2LOH54ZACTIB

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
Sparms 100% Organic Face SunscreenZINC OXIDE SUNSCREENVEGANIC SKN LIMITED4ae6b187-142b-e4a6-e063-6294a90af3652026-02-15WarningsExact identifier
ndc (package): 83252-143-21
ndc (package): 83252-143-15
ndc (package): 83252-143-01
ndc (product): 83252-143
ndc11 (package): 83252014315
ndc11 (package): 83252014321
ndc11 (package): 83252014301
spl id: 4ae6b10f-70ef-ed30-e063-6394a90a4af7
spl set id: 4ae6b187-142b-e4a6-e063-6294a90af365

Reported adverse events (FAERS/openFDA)#

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