FDA.reportPublic FDA data

Nux vomica

Product NDC
0220-3709
11-digit product format
002203709
Labeler code
0220
Product ID
0220-3709_09431201-e7dd-7245-e063-6394a90ab555
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
10 [hp_M]/10[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
IngredientStrength
STRYCHNOS NUX-VOMICA SEED10 [hp_M]/10[hp_M]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii269XH13919

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3709-412023-07-11C16284748780-1f386c64a-1f03-0266-e053-dadaa90a7c1aNux vomica 10M
0220-3709-412023-01-30C16284748780-1f386c64a-1f03-0266-e053-dadaa90a7c1aNux vomica 10M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3709-41Nux vomica10 [hp_M] in 1 TUBEPELLET103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3709NUX VOMICA (STRYCHNOS NUX-VOMICA SEED ) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231104_865a40bf-d8d9-9e4b-e053-2991aa0aadb6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3709-410022037094110 [hp_M] in 1 TUBE (0220-3709-41) 1983-03-030000-00-00NoNoCurrent