Home NDC 85211-002 Droptics Dry Eye Relief
Product NDC 85211-002
11-digit product format 852110002
Labeler code 85211
Product ID 85211-002_57323f74-e0a0-1ad8-e063-6294a90ad9d4
Type HUMAN OTC DRUG
Nonproprietary name Carboxymethylcellulose Sodium,Glycerin,Polysorbate 80
Dosage form LIQUID
Route OPHTHALMIC
Labeler Droptics LLC
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-02-01
Substance CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80
Active strength .5; 1; .5 g/100mL; g/100mL; g/100mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Glycerol [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Chemical Allergen [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 Droptics Dry Eye Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CARBOXYMETHYLCELLULOSE SODIUM .5 g/100mL GLYCERIN 1 g/100mL POLYSORBATE 80 .5 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K679OBS311 Internal UNII lookup PDC6A3C0OX Internal UNII lookup 6OZP39ZG8H Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1241471 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 85211-002-01 Droptics Dry Eye Relief 1 in 1 CARTON LIQUID 1 3 85211-002-01 Droptics Dry Eye Relief 5 mL in 1 BOTTLE, DROPPER LIQUID 5 3
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 85211-002-01 85211000201 1 BOTTLE, DROPPER in 1 CARTON (85211-002-01) / 5 mL in 1 BOTTLE, DROPPER 2025-02-01 No No Current 85211-002-02 85211000202 1 BOTTLE, DROPPER in 1 CARTON (85211-002-02) / 7 mL in 1 BOTTLE, DROPPER 2026-07-14 No No Current