FDA.reportPublic FDA data

Nux vomica

Product NDC
0220-3708
Requested package NDC
0220-3708-41
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
IngredientStrength
STRYCHNOS NUX-VOMICA SEED1 [hp_M]/[hp_M]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
269XH13919Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
865a27ab-6bb5-aef5-e053-2a91aa0a1f72Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-3708-412023-02-20C16284748780-1f386c64a-2002-0266-e053-dadaa90a7c1aNux vomica 1M
0220-3708-412023-01-30C16284748780-1f386c64a-2002-0266-e053-dadaa90a7c1aNux vomica 1M

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-3708-41Nux vomica1 [hp_M] in 1 TUBEPELLET13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-3708NUX VOMICA (STRYCHNOS NUX-VOMICA SEED ) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20231103_865a27ab-6bb5-aef5-e053-2a91aa0a1f72.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nux vomicaSTRYCHNOS NUX-VOMICA SEEDBoiron865a27ab-6bb5-aef5-e053-2a91aa0a1f722023-11-02Exact identifier
ndc (package): 0220-3708-41
ndc (product): 0220-3708
ndc11 (package): 00220370841

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-3708-41002203708411 [hp_M] in 1 TUBE (0220-3708-41) 1983-03-030000-00-00NoNoCurrent