BISMUTHUM SUBNITRICUM
- Product NDC
- 0220-0860
- 11-digit product format
- 002200860
- Labeler code
- 0220
- Product ID
- 0220-0860_39e8a434-0720-b2b0-e063-6294a90acd00
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BISMUTH SUBNITRATE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-01-01
- Substance
- BISMUTH SUBNITRATE
- Active strength
- 200 [kp_C]/200[kp_C]
- Pharmacologic classes
- Bismuth [CS], Bismuth [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BISMUTHUM SUBNITRICUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BISMUTH SUBNITRATE | 200 [kp_C]/200[kp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H19J064BA5 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-0860-41 | BISMUTHUM SUBNITRICUM | 200 [kp_C] in 1 TUBE | PELLET | 200 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-0860-41 | 00220086041 | 200 [kp_C] in 1 TUBE (0220-0860-41) | 2025-01-01 | No | No | Current |