Occuloplex G

Product NDC

43857-0141

11-digit product format

438570141

Labeler code

43857

Product ID

43857-0141_bf7c683b-0e1d-4d57-b9c3-d6ca2113e932

Type

HUMAN OTC DRUG

Nonproprietary name

Euphrasia Officinalis, Ginkgo Biloba, Petroselinum Sativum, Spigelia Anthelmia, Vaccinium Myrtillus, Ascorbic Acid, 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

2013-01-16

Marketing end

2021-08-31

Substance

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record