Nux vomica

Product NDC
0220-3702
11-digit product format
002203702
Labeler code
0220
Product ID
0220-3702_0941d99b-60e3-e61a-e063-6394a90a54e3
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
5 [hp_C]/5[hp_C]
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 SEED5 [hp_C]/5[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii269XH13919

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3702-41Nux vomica5 [hp_C] in 1 TUBEPELLET53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3702NUX VOMICA (STRYCHNOS NUX-VOMICA SEED ) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231104_86579f31-78a5-4581-e053-2a91aa0a5ce5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3702-41002203702415 [hp_C] in 1 TUBE (0220-3702-41) 1983-03-030000-00-00NoNoCurrent