Mercurius vivus

Product NDC
0220-3442
11-digit product format
002203442
Labeler code
0220
Product ID
0220-3442_f528dca9-23d9-b822-e053-2a95a90ae583
Type
HUMAN OTC DRUG
Nonproprietary name
MERCURY
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
MERCURY
Active strength
30 [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Mercurius vivus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MERCURY30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiFXS1BY2PGL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3442-412023-02-20C16284748780-1f386c649-f22f-0266-e053-dadaa90a7c1aMercurius vivus 30C
0220-3442-412023-01-30C16284748780-1f386c649-f22f-0266-e053-dadaa90a7c1aMercurius vivus 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3442-41Mercurius vivus30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3442MERCURIUS VIVUS (MERCURY) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230222_8641fbcd-0f35-29e6-e053-2a91aa0a5a82.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3442-410022034424130 [hp_C] in 1 TUBE (0220-3442-41) 1983-03-030000-00-00NoNoCurrent