FDA.reportPublic FDA data

Zincum sulphuricum

Product NDC
0220-5486
11-digit product format
002205486
Labeler code
0220
Product ID
0220-5486_21b581c7-06e9-dea3-e063-6294a90a91a3
Type
HUMAN OTC DRUG
Nonproprietary name
ZINC SULFATE HEPTAHYDRATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-01-01
Substance
ZINC SULFATE HEPTAHYDRATE
Active strength
200 [kp_C]/200[kp_C]
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Zincum sulphuricum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ZINC SULFATE HEPTAHYDRATE200 [kp_C]/200[kp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
N57JI2K7WPInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
21b581c7-06e8-dea3-e063-6294a90a91a3Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-5486-41Zincum sulphuricum200 [kp_C] in 1 TUBEPELLET2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-5486ZINCUM SULPHURICUM (ZINC SULFATE HEPTAHYDRATE) PELLET [BOIRON]1Current NDC, 1 package rows20240910_21b581c7-06e8-dea3-e063-6294a90a91a3.zip

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
Zincum sulphuricumZINC SULFATE HEPTAHYDRATEBoiron21b581c7-06e8-dea3-e063-6294a90a91a32024-09-09Exact identifier
ndc (product): 0220-5486

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0220-5486-4100220548641200 [kp_C] in 1 TUBE (0220-5486-41) 2024-01-01NoNoCurrent