Home NDC 50804-160 GoodSense Ultra Lubricant Eye Drops
Product NDC 50804-160
11-digit product format 508040160
Labeler code 50804
Product ID 50804-160_474511c4-1fbd-70b8-e063-6294a90af8e8
Type HUMAN OTC DRUG
Nonproprietary name polyethylene glycol 400, propylene glycol
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Geiss, Destin & Dunn, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-03
Substance PROPYLENE GLYCOL; POLYETHYLENE GLYCOL 400
Active strength .3; .4 g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
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 GoodSense Ultra Lubricant Eye Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PROPYLENE GLYCOL .3 g/100mL POLYETHYLENE GLYCOL 400 .4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 6DC9Q167V3 Internal UNII lookup B697894SGQ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 477589 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 50804-160-01 GoodSense Ultra Lubricant Eye Drops 1 in 1 CARTON SOLUTION 1 3 50804-160-01 GoodSense Ultra Lubricant Eye Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION 15 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50804-160 GOODSENSE ULTRA LUBRICANT EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL) SOLUTION [GEISS, DESTIN & DUNN, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20231224_9b45ebb5-c43b-c9fb-e053-2a95a90a3411.zip
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 Marketing start Marketing end Sample Exclude flag Status 50804-160-01 50804016001 1 BOTTLE, DROPPER in 1 CARTON (50804-160-01) / 15 mL in 1 BOTTLE, DROPPER 2020-01-03 0000-00-00 No No Current