FDA.reportPublic FDA data

Sunsolve MD Mineral Shade Amber 002

Manufacturer
Sunsolve MD Inc
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:16:00

Label at a glance#

ProductSunsolve MD Mineral Shade Amber 002
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sunsolve MD Mineral Shade Amber 002

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sunsolve MD Mineral Shade Amber 002

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Sunsolve MD Mineral Shade Amber 002

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Sunsolve MD Mineral Shade Amber 002

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Sunsolve MD Mineral Shade Amber 002

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Sunsolve MD Mineral Shade Amber 002

OTC - PURPOSE SECTION

purposepurpose

Sunsolve MD Mineral Shade Amber 002

WARNINGS SECTION

Warning LabelWarning Label

Sunsolve MD Mineral Shade Amber 002

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-135061023120071GTIN-13: 5061023120071
EAN-13: 5061023120071
GTIN storage (14 digits): 05061023120071		Sunsolve_MD_AMBER_PROTECT_002_AW_v10_Page_1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-402-01Sunsolve MD Mineral Shade Amber 00228 mL in 1 BOTTLE, PUMPLOTION284
84878-402-02Sunsolve MD Mineral Shade Amber 0021 in 1 CARTONLOTION14

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84878-40284878-402-01, 84878-402-02

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
TRILAURETH-4 PHOSPHATEM96W2OLL2VIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
ISODODECANEA8289P68Y2IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ZINC OXIDESOI2LOH54ZACTIB
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
GLYCERINPDC6A3C0OXIACT
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW)9KB5R958PBIACT
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
ALLANTOIN344S277G0ZIACT
PEG-10761NX2Q08YIACT
CAPRYLYL METHICONEQ95M2P1KJLIACT
DIMETHICONE92RU3N3Y1OIACT
LAURYL PEG-8 DIMETHICONE (300 CPS)ELL2U7K8T8IACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
CAPRYLYL GLYCOL00YIU5438UIACT

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
Sunsolve MD Mineral Shade Amber 002ZINC OXIDESunsolve MD Inc26e00001-9c68-0734-e063-6394a90a17872025-11-14WarningsExact identifier
ndc (package): 84878-402-01
ndc (package): 84878-402-02
ndc (product): 84878-402
ndc11 (package): 84878040202
ndc11 (package): 84878040201
spl id: 4392089e-99a0-ecf3-e063-6394a90ad61b
spl set id: 26e00001-9c68-0734-e063-6394a90a1787

Reported adverse events (FAERS/openFDA)#

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