Occuloplex G

Product NDC

43857-0461

11-digit product format

438570461

Labeler code

43857

Product ID

43857-0461_8e78973a-78fd-45e1-87b0-872a391e2c43

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Euphrasia Officinalis, Ginkgo Biloba, Petroselinum Sativum, Vaccinium Myrtillus, Ascorbic Acid, Spigelia Anthelmia, Eye (Suis), Germanium Sesquioxide, Lithium Metallicum, Ubidecarenonum, Aurum Metallicum, Bryonia (Alba), Hepar Sulphuris Calcareum, Phosphorus, Ruta Graveolens, Sulphur

Dosage form

LIQUID

Route

ORAL

Labeler

BioActive Nutritional, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2017-09-06

Marketing end

2022-10-16

Substance

EUPHRASIA STRICTA; GINKGO; PETROSELINUM CRISPUM; BILBERRY; ASCORBIC ACID; SPIGELIA ANTHELMIA; SUS SCROFA EYE; GERMANIUM SESQUIOXIDE; LITHIUM; UBIDECARENONE; GOLD; BRYONIA ALBA ROOT; CALCIUM SULFIDE; PHOSPHORUS; RUTA GRAVEOLENS FLOWERING TOP; SULFUR

Active strength

3 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

Pharmacologic classes

Vitamin C [EPC],Ascorbic Acid [CS],Mood Stabilizer [EPC],Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Allergens [CS],Cell-mediated Immunity [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record