BMNP NUX VOMICA

Product NDC
82969-5315
Requested package NDC
82969-5315-1
11-digit product format
829695315
Labeler code
82969
Product ID
82969-5315_5d679aa5-c2a8-b8cf-e063-6294a90ae023
Type
HUMAN OTC DRUG
Nonproprietary name
NUX VOMICA
Dosage form
GLOBULE
Route
ORAL
Labeler
Total Operations Management LLC DBA:Bestmade Natural Products Micro
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2026-06-01
Substance
STRYCHNOS NUX-VOMICA SEED
Active strength
30 [hp_C]/g
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
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
BMNP NUX VOMICA
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STRYCHNOS NUX-VOMICA SEED30 [hp_C]/g

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82969-5315-18296953150125 g in 1 BOTTLE, GLASS (82969-5315-1) 25 g2026-06-01NoNoCurrent