Home NDC 41163-540 Equaline Eye Drops A.C.
Product NDC 41163-540
11-digit product format 411630540
Labeler code 41163
Product ID 41163-540_0cfac3c3-6f4a-cc70-e063-6394a90a57b1
Type HUMAN OTC DRUG
Nonproprietary name tetrahydrozoline HCl, zinc sulfate
Dosage form SOLUTION
Route OPHTHALMIC
Labeler United Natural Foods, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-03-22
Substance TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE
Active strength .05; .25 g/100mL; g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Equaline Eye Drops A.C.
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TETRAHYDROZOLINE HYDROCHLORIDE .05 g/100mL ZINC SULFATE .25 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0YZT43HS7D Internal UNII lookup 89DS0H96TB Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1043249 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 41163-540-01 Equaline Eye Drops A.C. 1 in 1 CARTON SOLUTION 1 2 41163-540-01 Equaline Eye Drops A.C. 15 mL in 1 BOTTLE, DROPPER SOLUTION 15 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41163-540 EQUALINE EYE DROPS A.C. (TETRAHYDROZOLINE HCL, ZINC SULFATE) SOLUTION [UNITED NATURAL FOODS, INC.] 2 Current NDC, 2 package rows 20231224_f5f894f0-1ab0-4cad-e053-2995a90a7cba.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 Sample Exclude flag Status 41163-540-01 41163054001 1 BOTTLE, DROPPER in 1 CARTON (41163-540-01) / 15 mL in 1 BOTTLE, DROPPER 2023-03-22 No No Current