Ammonium Carbonicum
- Manufacturer
- Hahnemann Laboratories, Inc.
- Effective date
- 2020-10-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:13:22
Label at a glance#
ProductAmmonium Carbonicum
Active ingredientAMMONIUM CARBONATE
Label structure1 sections
Label contents#
Full prescribing information#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-940-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-fc74-a426-e053-dadaa90af4c2 | b0f10c1c-2dee-784c-e053-2995a90a64c4 |
| 63545-940-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-fc74-a426-e053-dadaa90af4c2 | b0f10c1c-2dee-784c-e053-2995a90a64c4 |
| 63545-940-03 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-fc74-a426-e053-dadaa90af4c2 | b0f10c1c-2dee-784c-e053-2995a90a64c4 |
| 63545-940-04 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-fc74-a426-e053-dadaa90af4c2 | b0f10c1c-2dee-784c-e053-2995a90a64c4 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-940-01 | Ammonium Carbonicum | 200 in 1 VIAL, GLASS | PELLET | 200 | 1 | |
| 63545-940-02 | Ammonium Carbonicum | 500 in 1 VIAL, GLASS | PELLET | 500 | 1 | |
| 63545-940-03 | Ammonium Carbonicum | 3000 in 1 BOTTLE, GLASS | PELLET | 3000 | 1 | |
| 63545-940-04 | Ammonium Carbonicum | 10000 in 1 BOTTLE, GLASS | PELLET | 10000 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Ammonium Carbonicum
- SUCROSE
- AMMONIUM CARBONATE
- CARBONATE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-940 | 63545-940-01, 63545-940-02, 63545-940-03, 63545-940-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| AMMONIUM CARBONATE | NJ5VT0FKLJ | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| b0f10c1c-2def-784c-e053-2995a90a64c4 | b0f10c1c-2dee-784c-e053-2995a90a64c4 | 2020-10-05 | b0f10c1c-2def-784c-e053-2995a90a64c4 b0f10c1c-2dee-784c-e053-2995a90a64c4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.



