FDA.reportPublic FDA data

Sunsolve MD Mineral Shade Quartz 001

Manufacturer
Sunsolve MD Inc
Effective date
2026-05-21
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:58:25

Label at a glance#

ProductSunsolve MD Mineral Shade Quartz 001
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sunsolve MD Mineral Shade Quartz 001

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sunsolve MD Mineral Shade Quartz 001

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Sunsolve MD Mineral Shade Quartz 001

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Sunsolve MD Mineral Shade Quartz 001

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Sunsolve MD Mineral Shade Quartz 001

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Sunsolve MD Mineral Shade Quartz 001

OTC - PURPOSE SECTION

purposepurpose

Sunsolve MD Mineral Shade Quartz 001

WARNINGS SECTION

Warning LabelWarning Label

Sunsolve MD Mineral Shade Quartz 001

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-401-01Sunsolve MD Mineral Shade Quartz 00128 mL in 1 BOTTLE, PUMPLOTION285
84878-401-02Sunsolve MD Mineral Shade Quartz 0011 in 1 CARTONLOTION15

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
84878-40184878-401-01, 84878-401-02

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
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
LAURYL PEG-8 DIMETHICONE (300 CPS)ELL2U7K8T8IACT
ZINC OXIDESOI2LOH54ZACTIB
DIMETHICONE92RU3N3Y1OIACT
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
ISODODECANEA8289P68Y2IACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
CAPRYLYL GLYCOL00YIU5438UIACT
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
LAURYL PEG-10 TRIS(TRIMETHYLSILOXY)SILYLETHYL DIMETHICONE35J49U6PZSIACT
ALLANTOIN344S277G0ZIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
FERRIC OXIDE RED1K09F3G675IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42025-11-14monthly-update2026-06-03 17:40:11

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
Sunsolve MD Mineral Shade Quartz 001ZINC OXIDESunsolve MD Inc26a54f00-d84d-8fe3-e063-6394a90a03e82026-05-21WarningsExact identifier
ndc (package): 84878-401-02
ndc (package): 84878-401-01
ndc (product): 84878-401
ndc11 (package): 84878040102
ndc11 (package): 84878040101
spl id: 525b87f5-f7d3-aa7e-e063-6294a90aa634
spl set id: 26a54f00-d84d-8fe3-e063-6394a90a03e8

Reported adverse events (FAERS/openFDA)#

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