FDA.reportPublic FDA data

Sunsolve MD Detox and Shield

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 Detox and Shield
Active ingredientZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

Sunsolve MD Detox and Shield

DOSAGE & ADMINISTRATION SECTION

Dosage and AdministrationDosage and Administration

Sunsolve MD Detox and Shield

INACTIVE INGREDIENT SECTION

Inactive ingredientsInactive ingredients

Sunsolve MD Detox and Shield

INDICATIONS & USAGE SECTION

Indications & usageIndications & usage

Sunsolve MD Detox and Shield

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsActive Ingredients

Sunsolve MD Detox and Shield

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

Sunsolve MD Detox and Shield

OTC - PURPOSE SECTION

purposepurpose

Sunsolve MD Detox and Shield

WARNINGS SECTION

Warning LabelWarning Label

Sunsolve MD Detox and Shield

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDP

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-135061023120002GTIN-13: 5061023120002
EAN-13: 5061023120002
GTIN storage (14 digits): 05061023120002		Sunsolve_MD_Detox Shield_AW_v15_Page_1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84878-998-01Sunsolve MD Detox and Shield48 mL in 1 BOTTLE, PUMPLOTION484
84878-998-02Sunsolve MD Detox and Shield1 in 1 CARTONLOTION14

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84878-99884878-998-01, 84878-998-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Name, UNII, Kind table
NameUNIIKind
JOJOBA OIL724GKU717MIACT
SCHINUS MOLLE OIL99O5U5NLK2IACT
ORYZA SATIVA WHOLE84IVV0906ZIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TOCOPHEROLR0ZB2556P8IACT
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
PROPANEDIOL5965N8W85TIACT
TETRASODIUM GLUTAMATE DIACETATE5EHL50I4MYIACT
SODIUM CHLORIDE451W47IQ8XIACT
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE687U3PEB2YIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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 Detox and ShieldZINC OXIDESunsolve MD Inc26f3886b-a3a5-c9b7-e063-6394a90af6c32025-11-14WarningsExact identifier
ndc (package): 84878-998-02
ndc (package): 84878-998-01
ndc (product): 84878-998
ndc11 (package): 84878099802
ndc11 (package): 84878099801
spl id: 4391f065-8427-cda3-e063-6394a90a38f4
spl set id: 26f3886b-a3a5-c9b7-e063-6394a90af6c3

Reported adverse events (FAERS/openFDA)#

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