Manganum Oxydatum Nigrum
- Manufacturer
- Hahnemann Laboratories, Inc.
- Effective date
- 2016-12-28
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:08:27
Label at a glance#
ProductManganum Oxydatum Nigrum
Active ingredientMANGANESE DIOXIDE
Label structure1 sections
Label contents#
Full prescribing information#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | 0000 | 44bcc8df-a813-010f-e054-00144ff88e88.jpg, Mang Ox N.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-663-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ba28-f424-e053-dadaa90a57ce | 44bd638a-3002-3d3a-e054-00144ff8d46c |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-663-01 | Manganum Oxydatum Nigrum | 240 [hp_C] in 1 VIAL, GLASS | PELLET | 240 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Manganum Oxydatum Nigrum
- MANGANESE DIOXIDE
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-663 | 63545-663-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MANGANESE DIOXIDE | TF219GU161 | ACTIB |
| SUCROSE | C151H8M554 | IACT |
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 |
|---|---|---|---|---|---|---|
| 44bd638a-3003-3d3a-e054-00144ff8d46c | 44bd638a-3002-3d3a-e054-00144ff8d46c | 2016-12-28 | 44bd638a-3003-3d3a-e054-00144ff8d46c 44bd638a-3002-3d3a-e054-00144ff8d46c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
