Bionica Combination

Product NDC

63083-9280

11-digit product format

630839280

Labeler code

63083

Product ID

63083-9280_6e81f806-be21-4e27-8cef-a7af5502cec9

Type

HUMAN OTC DRUG

Nonproprietary name

Bionica Combination

Dosage form

LIQUID

Route

ORAL

Labeler

Professional Complementary Health Formulas

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

1984-08-15

Marketing end

0000-00-00

Substance

APIS MELLIFERA; ARNICA MONTANA WHOLE; BAPTISIA TINCTORIA WHOLE; BENZOIC ACID; BRYONIA ALBA ROOT; COLCHICUM AUTUMNALE BULB; ECHINACEA ANGUSTIFOLIA WHOLE; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM PERFOLIATUM FLOWERING TOP; HOLOTHURIA SEA CUCUMBER; MERCURIALIS PERENNIS WHOLE; SOLANUM DULCAMARA WHOLE; SOLANUM NIGRUM TOP; TOXICODENDRON PUBESCENS LEAF

Active strength

4 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL

Pharmacologic classes

Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrogen Binding Agent [EPC], Standardized Insect Venom Allergenic Extract [EPC]

NDC exclude flag

No

Listing certified through

2023-12-31

Current FDA listing

Historical FDA.report record