Zincum Iodatum
- Manufacturer
- Hahnemann Laboratories, Inc.
- Effective date
- 2017-05-08
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:08:42
Label at a glance#
ProductZincum Iodatum
Active ingredientZINC IODIDE
Label structure1 sections
Label contents#
Full prescribing information#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | 00000 | 4f0672f8-0a4c-7210-e054-00144ff8d46c.jpg, Zinc-i.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 63545-690-01 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-da86-f424-e053-dadaa90a57ce | 4f064789-1641-3b21-e054-00144ff88e88 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 63545-690-01 | Zincum Iodatum | 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.
- Zincum Iodatum
- SUCROSE
- ZINC IODIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63545-690 | 63545-690-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| ZINC IODIDE | 762R7A0O0B | 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 |
|---|---|---|---|---|---|---|
| 4f064789-1642-3b21-e054-00144ff88e88 | 4f064789-1641-3b21-e054-00144ff88e88 | 2017-05-08 | 4f064789-1642-3b21-e054-00144ff88e88 4f064789-1641-3b21-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
