Ammonium carbonicum

Product NDC
0220-0241
11-digit product format
002200241
Labeler code
0220
Product ID
0220-0241_08041278-322b-35d1-e063-6394a90a748b
Type
HUMAN OTC DRUG
Nonproprietary name
AMMONIUM CARBONATE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
AMMONIUM CARBONATE
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
Ammonium carbonicum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
AMMONIUM CARBONATE30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
UniiNJ5VT0FKLJ

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0241-412023-10-18C16284748780-1f386c64a-337f-0266-e053-dadaa90a7c1aAmmonium carbonicum 30C
0220-0241-412023-01-30C16284748780-1f386c64a-337f-0266-e053-dadaa90a7c1aAmmonium carbonicum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0241-41Ammonium carbonicum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0241AMMONIUM CARBONICUM (AMMONIUM CARBONATE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20231019_84278e58-c313-f238-e053-2991aa0aa547.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0241-410022002414130 [hp_C] in 1 TUBE (0220-0241-41) 1983-03-030000-00-00NoNoCurrent