Home NDC 85766-165 GoodSense Eye Drops Advanced Relief Moisturizer
Product NDC 85766-165
11-digit product format 857660165
Labeler code 85766
Product ID 85766-165_4a353a2e-544c-8130-e063-6294a90a9491
Type HUMAN OTC DRUG
Nonproprietary name dextran, polyethylene glycol 400, povidone, tetrahydrozoline HCl
Dosage form SOLUTION
Route OPHTHALMIC
Labeler Sportpharm LLC
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-07
Substance POLYETHYLENE GLYCOL 400; TETRAHYDROZOLINE HYDROCHLORIDE; POVIDONE; DEXTRAN 70
Active strength 1; .05; 1; .1 g/100mL; g/100mL; g/100mL; g/100mL
Pharmacologic classes Increased Intravascular Volume [PE], Osmotic Activity [MoA], Plasma Volume Expander [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 GoodSense Eye Drops Advanced Relief Moisturizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POLYETHYLENE GLYCOL 400 1 g/100mL TETRAHYDROZOLINE HYDROCHLORIDE .05 g/100mL POVIDONE 1 g/100mL DEXTRAN 70 .1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 996202 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 85766-165-15 GoodSense Eye Drops Advanced Relief Moisturizer 15 mL in 1 CARTON SOLUTION 15 1 85766-165-15 GoodSense Eye Drops Advanced Relief Moisturizer 1 in 1 CARTON SOLUTION 1 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 85766-165-15 85766016515 1 CARTON in 1 CARTON (85766-165-15) / 15 mL in 1 CARTON 1 carton 2026-02-07 No No Current