FDA.reportPublic FDA data

Sunsovle MD Volumize and Restore

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 01:16:24

Label at a glance#

ProductSunsovle MD Volumize and Restore
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sunsovle MD Volumize and Restore

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sunsovle MD Volumize and Restore

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Sunsovle MD Volumize and Restore

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Sunsovle MD Volumize and Restore

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Sunsovle MD Volumize and Restore

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Sunsovle MD Volumize and Restore

OTC - PURPOSE SECTION

purposepurpose

Sunsovle MD Volumize and Restore

WARNINGS SECTION

Warning LabelWarning Label

Sunsovle MD Volumize and Restore

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-823-01Sunsovle MD Volumize and Restore50 mL in 1 BOTTLE, DROPPERLOTION504
84878-823-02Sunsovle MD Volumize and Restore1 in 1 CARTONLOTION14

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84878-82384878-823-01, 84878-823-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYL STEARATEC64RTC734WIACT
CAPRYLYL GLYCOL00YIU5438UIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
SQUALANEGW89575KF9IACT
ISODODECANEA8289P68Y2IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
ZINC OXIDESOI2LOH54ZACTIB
TOCOPHEROLR0ZB2556P8IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
COCO-CAPRYLATE4828G836N6IACT
ETHYL OLEATEZ2Z439864YIACT
RUTIN5G06TVY3R7IACT
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE255PIF62MSIACT
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS)59Z907ZB69IACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
LIMNANTHES ALBA (MEADOWFOAM) SEED OIL412ZHA4T4YIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES0C9AC7D6XUIACT
ETHYL PALMITATEIRD3M534ZMIACT
ISOHEXADECANE918X1OUF1EIACT
C13-15 ALKANE114P5I43UJIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
ETHYL LINOLEATEMJ2YTT4J8MIACT

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
Sunsovle MD Volumize and RestoreZINC OXIDESunsolve MD Inc26f3cdda-b990-15cb-e063-6394a90ade292025-11-14WarningsExact identifier
ndc (package): 84878-823-02
ndc (package): 84878-823-01
ndc (product): 84878-823
ndc11 (package): 84878082301
ndc11 (package): 84878082302
spl id: 4395b9eb-a4d0-37e7-e063-6394a90aeaa2
spl set id: 26f3cdda-b990-15cb-e063-6394a90ade29

Reported adverse events (FAERS/openFDA)#

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