NUX VOMICA

Product NDC
76472-3027
11-digit product format
764723027
Labeler code
76472
Product ID
76472-3027_2ddc5719-f994-6c57-e063-6294a90aa7bc
Type
HUMAN OTC DRUG
Nonproprietary name
NUX VOMICA
Dosage form
PELLET
Route
SUBLINGUAL
Labeler
SEVENE USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2011-11-23
Substance
STRYCHNOS NUX-VOMICA SEED
Active strength
200 [kp_C]/1
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
Brand name suffix
200ck
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STRYCHNOS NUX-VOMICA SEED200 [kp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii269XH13919

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76472-3027-1NUX VOMICA200ck80 in 1 CYLINDERPELLET804

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76472-3027NUX VOMICA 200CK (NUX VOMICA) PELLET [SEVENE USA]4Current NDC, Legacy NDC, 1 package rows20250213_cf892234-de79-37e1-e053-2995a90a1c39.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
76472-3027-17647230270180 PELLET in 1 CYLINDER (76472-3027-1) 80 pellet2011-11-230000-00-00NoNoCurrent