Nux vomica
- Product NDC
- 0220-3708
- 11-digit product format
- 002203708
- Labeler code
- 0220
- Product ID
- 0220-3708_093227d6-e122-8765-e063-6394a90aeef8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- STRYCHNOS NUX-VOMICA SEED
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- STRYCHNOS NUX-VOMICA SEED
- Active strength
- 1 [hp_M]/[hp_M]
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nux vomica
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| STRYCHNOS NUX-VOMICA SEED | 1 [hp_M]/[hp_M] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 269XH13919 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-3708-41 | Nux vomica | 1 [hp_M] in 1 TUBE | PELLET | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-3708 | NUX VOMICA (STRYCHNOS NUX-VOMICA SEED ) PELLET [BOIRON] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231103_865a27ab-6bb5-aef5-e053-2a91aa0a1f72.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-3708-41 | 00220370841 | 1 [hp_M] in 1 TUBE (0220-3708-41) | 1983-03-03 | 0000-00-00 | No | No | Current |