NUX VOMICA

Product NDC
15631-2868
11-digit product format
156312868
Labeler code
15631
Product ID
15631-2868_1a223bf8-fc34-dbcd-e063-6394a90a263e
Type
HUMAN OTC DRUG
Nonproprietary name
NUX VOMICA
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-05-23
Substance
STRYCHNOS NUX-VOMICA SEED
Active strength
3 [hp_X]/mL
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 SEED3 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii269XH13919

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-2868-0NUX VOMICA10 mL in 1 BOTTLELIQUID101
15631-2868-1NUX VOMICA30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-2868NUX VOMICA LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Current NDC, 2 package rows20240606_1a223bf8-fc33-dbcd-e063-6394a90a263e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
15631-2868-01563128680010 mL in 1 BOTTLE (15631-2868-0) 10 ml2024-05-23NoNoCurrent
15631-2868-11563128680130 mL in 1 BOTTLE (15631-2868-1) 30 ml2024-05-23NoNoCurrent