BM Nux Vomica

Product NDC
85816-5079
11-digit product format
858165079
Labeler code
85816
Product ID
85816-5079_38e1f158-1879-3b86-e063-6294a90a396f
Type
HUMAN OTC DRUG
Nonproprietary name
Nux Vomica
Dosage form
GLOBULE
Route
ORAL
Labeler
BM Private Limited
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-01
Substance
STRYCHNOS NUX-VOMICA SEED
Active strength
30 [hp_C]/1000mg
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
BM Nux Vomica
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STRYCHNOS NUX-VOMICA SEED30 [hp_C]/1000mg

Harmonized Identifiers#

Field, Values table
FieldValues
Unii269XH13919

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85816-5079-1BM Nux Vomica30000 mg in 1 BOTTLE, GLASSGLOBULE300001

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85816-5079-18581650790130000 mg in 1 BOTTLE, GLASS (85816-5079-1) 30000 mg2015-01-01NoNoHistorical