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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
269XH13919STRYCHNOS NUX-VOMICA SEED8046-97-7STRYCHNOS NUX-VOMICA SEED

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
15631-2868-01563128680010 mL in 1 BOTTLE (15631-2868-0) 10 ml2024-05-23NoNoHistorical
15631-2868-11563128680130 mL in 1 BOTTLE (15631-2868-1) 30 ml2024-05-23NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NUX VOMICA - Rxhomeo Private Limited d.b.a. Rxhomeo, IncRxhomeo Private Limited d.b.a. Rxhomeo, Inc2024-06-05HUMAN OTC DRUG LABEL1