Home NDC 64108-212 MINIDROPS
Product NDC 64108-212
11-digit product format 641080212
Labeler code 64108
Product ID 64108-212_49f38ac7-54c3-3b87-e063-6294a90a65a5
Type HUMAN OTC DRUG
Nonproprietary name Lubricant eye drops
Dosage form LIQUID
Route OPHTHALMIC
Labeler Optics Laboratory, Inc
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 1991-04-01
Substance POVIDONE, UNSPECIFIED; POLYVINYL ALCOHOL
Active strength 6; 14 mg/mL; mg/mL
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 MINIDROPS
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POVIDONE, UNSPECIFIED 6 mg/mL POLYVINYL ALCOHOL 14 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FZ989GH94E Internal UNII lookup 532B59J990 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 359969 Internal RxNorm lookup 1046287 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 64108-212-10 MINIDROPS 0.5 mL in 1 VIAL, SINGLE-USE LIQUID 0.5 9 64108-212-12 MINIDROPS 30 in 1 BOX LIQUID 30 9 64108-212-13 MINIDROPS 5 in 1 BOX LIQUID 5 9 64108-212-65 MINIDROPS 65 in 1 BOX LIQUID 65 9
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64108-212 MINIDROPS (LUBRICANT EYE DROPS) LIQUID [OPTICS LABORATORY, INC] 7 Current NDC, Legacy NDC, 4 package rows 20241218_c13c5f91-50df-471c-a7c9-1747a2ac1250.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 64108-212-10 64108021210 .5 mL in 1 VIAL, SINGLE-USE (64108-212-10) 1991-04-01 No No Current 64108-212-12 64108021212 30 VIAL, SINGLE-USE in 1 BOX (64108-212-12) / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10) 1991-04-01 0000-00-00 No No Current 64108-212-13 64108021213 5 VIAL, SINGLE-USE in 1 BOX (64108-212-13) / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10) 1991-04-01 0000-00-00 No No Current 64108-212-65 64108021265 65 VIAL, SINGLE-USE in 1 BOX (64108-212-65) / .5 mL in 1 VIAL, SINGLE-USE (64108-212-10) 1991-04-01 0000-00-00 No No Current