Home NDC 0065-0408 Alcon Tears Lubricant Eye Drops
Product NDC 0065-0408
11-digit product format 000650408
Labeler code 0065
Product ID 0065-0408_ea6245c6-1d3b-4fac-a0b5-b576f9f53af5
Type HUMAN OTC DRUG
Nonproprietary name hypromellose 2910
Dosage form SOLUTION/ DROPS
Route OPHTHALMIC
Labeler Alcon Laboratories, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-03-01
Substance HYPROMELLOSE 2910 (4000 MPA.S)
Active strength 5 mg/mL
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 Alcon Tears Lubricant Eye Drops
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HYPROMELLOSE 2910 (4000 MPA.S) 5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination RN3152OP35 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 142002 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0065-0408-72 Alcon Tears Lubricant Eye Drops 15 mL in 1 BOTTLE, DROPPER SOLUTION/ DROPS 15 3 0065-0408-72 Alcon Tears Lubricant Eye Drops 1 in 1 CARTON SOLUTION/ DROPS 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0065-0408 ALCON TEARS LUBRICANT EYE DROPS (HYPROMELLOSE 2910) SOLUTION/ DROPS [ALCON LABORATORIES, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20231215_89302e2b-882b-48d5-8df7-be37859b48ba.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 0065-0408-72 00065040872 1 BOTTLE, DROPPER in 1 CARTON (0065-0408-72) / 15 mL in 1 BOTTLE, DROPPER 2022-03-01 0000-00-00 No No Current