Home NDC 69842-474 CVS Gentle Tears
Product NDC 69842-474
11-digit product format 698420474
Labeler code 69842
Product ID 69842-474_47491cc4-1a60-464e-e063-6394a90a2770
Type HUMAN OTC DRUG
Nonproprietary name Dextran 70, Hypromellose
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler CVS Pharmacy, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance HYPROMELLOSE, UNSPECIFIED; DEXTRAN 70
Active strength .3; .1 g/100mL; g/100mL
Pharmacologic classes Increased Intravascular Volume [PE], Osmotic Activity [MoA], Plasma Volume Expander [EPC]
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 Gentle Tears
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYPROMELLOSE, UNSPECIFIED .3 g/100mL DEXTRAN 70 .1 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3NXW29V3WO Internal UNII lookup 7SA290YK68 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 309714 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 69842-474-01 CVS Gentle Tears 35 in 1 BOX SOLUTION/ DROPS 35 3 69842-474-01 CVS Gentle Tears 0.4 mL in 1 VIAL, SINGLE-USE SOLUTION/ DROPS 0.4 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-474 CVS GENTLE TEARS (DEXTRAN 70, HYPROMELLOSE) SOLUTION/ DROPS [CVS PHARMACY, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20240103_9b1ea0eb-c34f-6603-e053-2995a90a6a95.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 69842-474-01 69842047401 35 VIAL, SINGLE-USE in 1 BOX (69842-474-01) / .4 mL in 1 VIAL, SINGLE-USE 2020-01-01 0000-00-00 No No Current