HA HP

Product NDC
43857-0285
11-digit product format
438570285
Labeler code
43857
Product ID
43857-0285_2a7cee16-82ee-436e-8fec-c22681b40d36
Type
HUMAN OTC DRUG
Nonproprietary name
Belladonna, Bryonia (Alba), Gelsemium Sempervirens, Glonoinum, Melilotus Officinalis, Nux Vomica, Silicea, Spigelia Anthelmia
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-08-22
Substance
ATROPA BELLADONNA; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; MELILOTUS OFFICINALIS TOP; NITROGLYCERIN; SILICON DIOXIDE; SODIUM CHLORIDE; SPIGELIA ANTHELMIA; STRYCHNOS NUX-VOMICA SEED
Active strength
30; 30; 30; 30; 30; 30; 30; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vasodilation [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WQZ3G9PF0HATROPA BELLADONNAATROPA BELLADONNA
T7J046YI2BBRYONIA ALBA ROOTBRYONIA ALBA ROOT
639KR60Q1QGELSEMIUM SEMPERVIRENS ROOTGELSEMIUM SEMPERVIRENS ROOT
GM6P02J2DXMELILOTUS OFFICINALIS TOPMELILOTUS OFFICINALIS TOP
G59M7S0WS3NITROGLYCERIN55-63-0NITROGLYCERIN
ETJ7Z6XBU4SILICON DIOXIDE7631-86-9SILICON DIOXIDE
451W47IQ8XSODIUM CHLORIDE7647-14-5SODIUM CHLORIDE
WYT05213GESPIGELIA ANTHELMIASPIGELIA ANTHELMIA
269XH13919STRYCHNOS NUX-VOMICA SEED8046-97-7STRYCHNOS NUX-VOMICA SEED

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
43857-0285-14385702850130 mL in 1 BOTTLE, DROPPER (43857-0285-1) 30 ml2018-07-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug Facts:BioActive Nutritional, Inc. | Apotheca Company2018-07-06HUMAN OTC DRUG LABEL2