FDA.reportPublic FDA data

PUR 4-in-1 Skin Tint LN2

Manufacturer
PUR Minerals
Effective date
2025-09-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:14:40

Label at a glance#

ProductPUR 4-in-1 Skin Tint LN2
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

PUR 4-in-1 Skin Tint LN2

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

PUR 4-in-1 Skin Tint LN2

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

PUR 4-in-1 Skin Tint LN2

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

PUR 4-in-1 Skin Tint LN2

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

PUR 4-in-1 Skin Tint LN2

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

PUR 4-in-1 Skin Tint LN2

OTC - PURPOSE SECTION

PurposePurpose

PUR 4-in-1 Skin Tint LN2

WARNINGS SECTION

WarningWarning

PUR 4-in-1 Skin Tint LN2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67345-0050-0PUR 4-in-1 Skin Tint LN21 in 1 CARTONLOTION12
67345-0050-1PUR 4-in-1 Skin Tint LN230 mL in 1 BOTTLELOTION302

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67345-005067345-0050-1, 67345-0050-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
LAURYL PEG-8 DIMETHICONE (300 CPS)ELL2U7K8T8IACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
TOCOPHEROLR0ZB2556P8IACT
RETINOLG2SH0XKK91IACT
ISODODECANEA8289P68Y2IACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
CERAMIDE APF1X8L2B00JIACT
LACTIC ACID33X04XA5ATIACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
ORYZA SATIVA (RICE) BRANR60QEP13ICIACT
SODIUM HYDROXIDE55X04QC32IIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL8LGU7VM393IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
CAPRYLYL GLYCOL00YIU5438UIACT
ALLANTOIN344S277G0ZIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
NIACINAMIDE25X51I8RD4IACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
DIMETHICONE92RU3N3Y1OIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT

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
PUR 4-in-1 Skin Tint LN2ZINC OXIDEPUR Minerals3f069dfe-289d-8d3b-e063-6394a90a04962025-09-24WarningsExact identifier
ndc (package): 67345-0050-0
ndc (package): 67345-0050-1
ndc (product): 67345-0050
ndc11 (package): 67345005001
ndc11 (package): 67345005000
spl id: 3f904914-0a04-7c80-e063-6394a90aa18e
spl set id: 3f069dfe-289d-8d3b-e063-6394a90a0496

Reported adverse events (FAERS/openFDA)#

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