Home FDA labels b5928f0a-8a3c-6765-e053-2995a90a9011 Eye Floaters 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 Eye Floaters
Generic name ALOE, CARBO VEGETABILIS, CAUSTICUM, CHELIDONIUM MAJUS, CHOLESTERINUM, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, CYCLAMEN EUROPAEUM, GELSEMIUM SEMPERVIRENS, KALI CARBONICUM, MERCURIUS VIVUS, PHOSPHORUS, PHYSOSTIGMA VENENOSUM, PRUNUS SPINOSA, SENEGA OFFICINALIS, SEPIA, SULPHUR, TABACUM.
Manufacturer Newton Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 9a00f7a3-aa76-78ac-e053-2995a90a8c66
SPL ID b5928f0a-8a3c-6765-e053-2995a90a9011
Version 2
Effective date 2020-12-03
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:47:53 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 · 27 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Eye Floaters openfda.brand_name generic name ALOE, CARBO VEGETABILIS, CAUSTICUM, CHELIDONIUM MAJUS, CHOLESTERINUM, CINCHONA OFFICINALIS, COLCHICUM AUTUMNALE, CYCLAMEN EUROPAEUM, GELSEMIUM SEMPERVIRENS, KALI CARBONICUM, MERCURIUS VIVUS, PHOSPHORUS, PHYSOSTIGMA VENENOSUM, PRUNUS SPINOSA, SENEGA OFFICINALIS, SEPIA, SULPHUR, TABACUM. openfda.generic_name manufacturer name Newton Laboratories, Inc. openfda.manufacturer_name ndc package 55714-4774-1 openfda.package_ndc ndc product 55714-4774 openfda.product_ndc ndc11 package 55714477401 derived:openfda.package_ndc spl id b5928f0a-8a3c-6765-e053-2995a90a9011 id spl set id 9a00f7a3-aa76-78ac-e053-2995a90a8c66 set_id unii 2P3VWU3H10 openfda.unii unii 27YLU75U4W openfda.unii unii C9642I91WL openfda.unii unii 7E889U5RNN openfda.unii unii DD5FO1WKFU openfda.unii unii 993QHL78E6 openfda.unii unii G728143D8Q openfda.unii unii QDL83WN8C2 openfda.unii unii FXS1BY2PGL openfda.unii unii 639KR60Q1Q openfda.unii unii 6YR2608RSU openfda.unii unii CJV9E9IIOA openfda.unii unii BQN1B9B9HA openfda.unii unii 53Y84VPS2W openfda.unii unii 97C5T2UQ7J openfda.unii unii V5VD430YW9 openfda.unii unii S003A158SB openfda.unii unii 70FD1KFU70 openfda.unii unii M7T6H7D4IF 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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.