FDA.reportPublic FDA data

Sunsolve MD Volumize and Condition Lip

Manufacturer
Sunsolve MD
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:16:03

Label at a glance#

ProductSunsolve MD Volumize and Condition Lip
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sunsolve MD Volumize and Condition Lip

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sunsolve MD Volumize and Condition Lip

INACTIVE INGREDIENT SECTION

Inactive IngredientInactive Ingredient

Sunsolve MD Volumize and Condition Lip

INDICATIONS & USAGE SECTION

Indications and UsageIndications and Usage

Sunsolve MD Volumize and Condition Lip

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

Sunsolve MD Volumize and Condition Lip

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenKeep out of reach of children

Sunsolve MD Volumize and Condition Lip

OTC - PURPOSE SECTION

PurposePurpose

Sunsolve MD Volumize and Condition Lip

WARNINGS SECTION

WarningWarning

Sunsolve MD Volumize and Condition Lip

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-107-01Sunsolve MD Volumize and Condition Lip4.5 mL in 1 BOTTLE, WITH APPLICATORLOTION4.52
84878-107-02Sunsolve MD Volumize and Condition Lip1 in 1 CARTONLOTION12

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84878-10784878-107-01, 84878-107-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE255PIF62MSIACT
ISOHEXADECANE918X1OUF1EIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
FERRIC OXIDE RED1K09F3G675IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
CAPRYLYL GLYCOL00YIU5438UIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
LIMNANTHES ALBA (MEADOWFOAM) SEED OIL412ZHA4T4YIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
MICAV8A1AW0880IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
METHYLPROPANEDIOLN8F53B3R4RIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
SQUALANEGW89575KF9IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
PHENYLPROPANOL0F897O3O4MIACT

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 Volumize and Condition LipZINC OXIDESunsolve MD396b7462-d597-4bf7-e063-6394a90ab58d2025-11-14WarningsExact identifier
ndc (package): 84878-107-02
ndc (package): 84878-107-01
ndc (product): 84878-107
ndc11 (package): 84878010701
ndc11 (package): 84878010702
spl id: 4395b691-2e0f-0acc-e063-6294a90adfb4
spl set id: 396b7462-d597-4bf7-e063-6394a90ab58d

Reported adverse events (FAERS/openFDA)#

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