Kreosotum
- Product NDC
- 0220-2946
- 11-digit product format
- 002202946
- Labeler code
- 0220
- Product ID
- 0220-2946_0a0e30cc-ad75-8cf3-e063-6394a90a974d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WOOD CREOSOTE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- WOOD CREOSOTE
- Active strength
- 12 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Kreosotum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WOOD CREOSOTE | 12 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3JYG22FD73 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-2946-41 | Kreosotum | 80 in 1 TUBE | PELLET | 80 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-2946 | KREOSOTUM (WOOD CREOSOTE) PELLET [BOIRON] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231114_19fe8720-7c5e-11e6-85cf-424c58303031.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-2946-41 | 00220294641 | 80 PELLET in 1 TUBE (0220-2946-41) | 80 pellet | 1983-03-03 | 0000-00-00 | No | No | Current |