Home NDC 69842-611 CVS Astringent Eye
Product NDC 69842-611
11-digit product format 698420611
Labeler code 69842
Product ID 69842-611_47491040-0b87-ee67-e063-6294a90a47d4
Type HUMAN OTC DRUG
Nonproprietary name Tetrahydrozoline HCl, Zinc sulfate
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler CVS Pharmacy, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2007-11-01
Substance TETRAHYDROZOLINE HYDROCHLORIDE; ZINC SULFATE
Active strength 50; 250 mg/100mL; mg/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 CVS Astringent Eye
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TETRAHYDROZOLINE HYDROCHLORIDE 50 mg/100mL ZINC SULFATE 250 mg/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 69842-611-01 CVS Astringent Eye 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 5 69842-611-01 CVS Astringent Eye 1 in 1 BOX SOLUTION/ DROPS 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-611 CVS ASTRINGENT EYE (TETRAHYDROZOLINE HCL, ZINC SULFATE) SOLUTION/ DROPS [CVS PHARMACY, INC.] 4 Current NDC, Legacy NDC, 2 package rows 20231224_07e1a56b-fdad-408d-bf5a-7a0144ece131.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 69842-611-01 69842061101 1 BOTTLE, DROPPER in 1 BOX (69842-611-01) / 15 mL in 1 BOTTLE, DROPPER 2007-11-01 0000-00-00 No No Current