Home FDA labels c74fbdf1-ce96-46a3-a054-6a2f1113805e Occuloplex G openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Occuloplex G
Generic name EUPHRASIA OFFICINALIS, GINKGO BILOBA, PETROSELINUM SATIVUM, VACCINIUM MYRTILLUS, ASCORBICUM ACIDUM, SPIGELIA ANTHELMIA, EYE (SUIS), GERMANIUM SESQUIOXIDE, UBIDECARENONUM, AURUM METALLICUM, BRYONIA (ALBA), HEPAR SULPHURIS CALCAREUM, PHOSPHORUS, RUTA GRAVEOLENS, SULPHUR, LITHIUM METALLICUM
Manufacturer BioActive Nutritional, Inc.
Product type HUMAN OTC DRUG
SPL set ID c982e701-129c-4b55-b8e6-ff0517838492
SPL ID c74fbdf1-ce96-46a3-a054-6a2f1113805e
Version 2
Effective date 2024-05-02
Source export date 2026-10-12
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:46:27 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Occuloplex G openfda.brand_name generic name EUPHRASIA OFFICINALIS, GINKGO BILOBA, PETROSELINUM SATIVUM, VACCINIUM MYRTILLUS, ASCORBICUM ACIDUM, SPIGELIA ANTHELMIA, EYE (SUIS), GERMANIUM SESQUIOXIDE, UBIDECARENONUM, AURUM METALLICUM, BRYONIA (ALBA), HEPAR SULPHURIS CALCAREUM, PHOSPHORUS, RUTA GRAVEOLENS, SULPHUR, LITHIUM METALLICUM openfda.generic_name manufacturer name BioActive Nutritional, Inc. openfda.manufacturer_name ndc package 43857-0513-1 openfda.package_ndc ndc product 43857-0513 openfda.product_ndc ndc11 package 43857051301 derived:openfda.package_ndc spl id c74fbdf1-ce96-46a3-a054-6a2f1113805e id spl set id c982e701-129c-4b55-b8e6-ff0517838492 set_id unii 27YLU75U4W openfda.unii unii EJ27X76M46 openfda.unii unii C9642I91WL openfda.unii unii 96WE91N25T openfda.unii unii N94C2U587S openfda.unii unii 79Y1949PYO openfda.unii unii PQ6CK8PD0R openfda.unii unii X3AOK514E6 openfda.unii unii WYT05213GE openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii 1WZA4Y92EX openfda.unii unii 19FUJ2C58T openfda.unii unii 9P2U39H18W openfda.unii unii 9FN79X2M3F openfda.unii unii 1MBW07J51Q openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in cool, dry place.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.