Zincum sulphuricum
- Product NDC
- 0220-5486
- 11-digit product format
- 002205486
- Labeler code
- 0220
- Product ID
- 0220-5486_21b581c7-06e9-dea3-e063-6294a90a91a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC SULFATE HEPTAHYDRATE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-01-01
- Substance
- ZINC SULFATE HEPTAHYDRATE
- Active strength
- 200 [kp_C]/200[kp_C]
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zincum sulphuricum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC SULFATE HEPTAHYDRATE | 200 [kp_C]/200[kp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N57JI2K7WP |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-5486-41 | Zincum sulphuricum | 200 [kp_C] in 1 TUBE | PELLET | 200 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-5486 | ZINCUM SULPHURICUM (ZINC SULFATE HEPTAHYDRATE) PELLET [BOIRON] | 1 | Current NDC, 1 package rows | 20240910_21b581c7-06e8-dea3-e063-6294a90a91a3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-5486-41 | 00220548641 | 200 [kp_C] in 1 TUBE (0220-5486-41) | 2024-01-01 | No | No | Current |