FDA.reportPublic FDA data

Mercurius 21X

Product NDC
48951-8385
11-digit product format
489518385
Labeler code
48951
Product ID
48951-8385_cf584125-a0de-49e5-e053-2a95a90a0bd0
Type
HUMAN OTC DRUG
Nonproprietary name
Mercurius 21X
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
MERCURY
Active strength
21 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-8385IInactivated by FDA2026-08-17
excluded packagepackage48951-838548951-8385-1IInactivated by FDA2026-08-17

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct48951-8385DDiscontinued by firmexcluded / ndc_excluded.zip557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage48951-838548951-8385-1DDiscontinued by firmexcluded / ndc_excluded.zip557ba5c1ecfa…9c80585c8c6e…

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8385-1Mercurius 21X60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8385MERCURIUS 21X LIQUID [URIEL PHARMACY, INC.]3Legacy NDC, 1 package rows20240926_cf584125-a0dd-49e5-e053-2a95a90a0bd0.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8385-14895183850160 mL in 1 BOTTLE, DROPPER (48951-8385-1) 60 ml2009-09-010000-00-00NoNoCurrent