FDA.reportPublic FDA data

Sunsolve MD Firm and Replenish

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 01:16:01

Label at a glance#

ProductSunsolve MD Firm and Replenish
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sunsolve MD Firm and Replenish

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sunsolve MD Firm and Replenish

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Sunsolve MD Firm and Replenish

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Sunsolve MD Firm and Replenish

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Sunsolve MD Firm and Replenish

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Sunsolve MD Firm and Replenish

OTC - PURPOSE SECTION

purposepurpose

Sunsolve MD Firm and Replenish

WARNINGS SECTION

Warning LabelWarning Label

Sunsolve MD Firm and ReplenishSunsolve MD Firm and Replenish

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-135061023120019GTIN-13: 5061023120019
EAN-13: 5061023120019
GTIN storage (14 digits): 05061023120019		41478 Sunsolve - E - Firm Replenish v2_Page_1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-199-01Sunsolve MD Firm and Replenish48 mL in 1 BOTTLE, PUMPLOTION484
84878-199-02Sunsolve MD Firm and Replenish1 in 1 CARTONLOTION14
84878-199-03Sunsolve MD Firm and Replenish13 mL in 1 BOTTLE, PUMPLOTION134
84878-199-04Sunsolve MD Firm and Replenish1 in 1 CARTONLOTION14

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84878-19984878-199-01, 84878-199-02, 84878-199-03, 84878-199-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM HYALURONATEYSE9PPT4THIACT
TOCOPHEROLR0ZB2556P8IACT
PHENOXYETHANOLHIE492ZZ3TIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
CERAMIDE NP4370DF050BIACT
JOJOBA OIL724GKU717MIACT
ORYZA SATIVA WHOLE84IVV0906ZIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
CAPRYLYL GLYCOL00YIU5438UIACT
COCO-CAPRYLATE4828G836N6IACT
NYLON-12446U8J075BIACT
PHENYLPROPANOL0F897O3O4MIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
METHYLPROPANEDIOLN8F53B3R4RIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
ALLANTOIN344S277G0ZIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
ROSMARINUS OFFICINALIS FLOWERNR1A27F29OIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
ZINC OXIDESOI2LOH54ZACTIB
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
NIACINAMIDE25X51I8RD4IACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
PROPANEDIOL5965N8W85TIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
SODIUM CHLORIDE451W47IQ8XIACT
FERRIC OXIDE RED1K09F3G675IACT

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 Firm and ReplenishZINC OXIDESunsolve MD Inc26f3417b-9ea4-e577-e063-6294a90ae53c2025-11-14WarningsExact identifier
ndc (package): 84878-199-03
ndc (package): 84878-199-04
ndc (package): 84878-199-01
ndc (package): 84878-199-02
ndc (product): 84878-199
ndc11 (package): 84878019901
ndc11 (package): 84878019902
ndc11 (package): 84878019903
ndc11 (package): 84878019904
spl id: 439594af-fc39-cec4-e063-6294a90a455f
spl set id: 26f3417b-9ea4-e577-e063-6294a90ae53c

Reported adverse events (FAERS/openFDA)#

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