Home NDC 59390-184 Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent
Product NDC 59390-184
11-digit product format 593900184
Labeler code 59390
Product ID 59390-184_fc39d7b1-cea0-4702-89bd-bf63adbeb675
Type HUMAN OTC DRUG
Nonproprietary name Sodium Chloride
Dosage form OINTMENT
Route OPHTHALMIC
Labeler Altaire Pharmaceuticals Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2004-03-30
Substance SODIUM CHLORIDE
Active strength 50 mg/g
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM CHLORIDE 50 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 451W47IQ8X Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1298435 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59390-184-50 Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent 1 in 1 BOX OINTMENT 1 1 59390-184-50 Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent 3.5 g in 1 TUBE OINTMENT 3.5 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 6 of 25 · 494 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59390-184-50 59390018450 1 TUBE in 1 BOX (59390-184-50) / 3.5 g in 1 TUBE 1 tube 2004-03-30 No No Current