FDA.reportPublic FDA data

Yon-Ka 50 Mineral Fluid

Manufacturer
Laboratoire MULTALER Yon-Ka
Effective date
2026-01-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:31:16

Label at a glance#

ProductYon-Ka 50 Mineral Fluid
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Yon-Ka 50 Mineral Fluid

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Yon-Ka 50 Mineral Fluid

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Yon-Ka 50 Mineral Fluid

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Yon-Ka 50 Mineral Fluid

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Yon-Ka 50 Mineral Fluid

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Yon-Ka 50 Mineral Fluid

OTC - PURPOSE SECTION

PurposePurpose

Yon-Ka 50 Mineral Fluid

WARNINGS SECTION

WarningWarning

Yon-Ka 50 Mineral Fluid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51191-2667-1Yon-Ka 50 Mineral Fluid60 mL in 1 TUBELOTION601
51191-2667-2Yon-Ka 50 Mineral Fluid1 in 1 CARTONLOTION11
51191-2667-3Yon-Ka 50 Mineral Fluid30 mL in 1 TUBELOTION301
51191-2667-4Yon-Ka 50 Mineral Fluid1 in 1 CARTONLOTION11

Products#

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

DailyMed product names page 1 of 1 · 28 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51191-266751191-2667-1, 51191-2667-2, 51191-2667-3, 51191-2667-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM HYDROXIDE55X04QC32IIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
CAPRYLYL GLYCOL00YIU5438UIACT
DIMETHICONE 200RGS4T2AS00IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
LAURYL PEG-8 DIMETHICONE (300 CPS)ELL2U7K8T8IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
ISODODECANEA8289P68Y2IACT
ZINC OXIDESOI2LOH54ZACTIB
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALLANTOIN344S277G0ZIACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
C13-15 ALKANE114P5I43UJIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CALCIUM SODIUM BOROSILICATE4MM76N4WMYIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
SILICON DIOXIDEETJ7Z6XBU4IACT

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
Yon-Ka 50 Mineral FluidZINC OXIDELaboratoire MULTALER Yon-Ka47a8c8b2-30ff-0d40-e063-6294a90ac4612026-01-05WarningsExact identifier
ndc (package): 51191-2667-2
ndc (package): 51191-2667-3
ndc (package): 51191-2667-1
ndc (package): 51191-2667-4
ndc (product): 51191-2667
ndc11 (package): 51191266704
ndc11 (package): 51191266701
ndc11 (package): 51191266703
ndc11 (package): 51191266702
spl id: 47a8c7b9-df91-1569-e063-6294a90a2fd4
spl set id: 47a8c8b2-30ff-0d40-e063-6294a90ac461

Reported adverse events (FAERS/openFDA)#

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