Home NDC 50989-476 Vedlube
Product NDC 50989-476
11-digit product format 509890476
Labeler code 50989
Product ID 50989-476_815352b9-bd2f-4b38-a788-295dc677729c
Type HUMAN OTC DRUG
Nonproprietary name Mineral Oil and White Petrolatum Lubricant Eye Ointment
Dosage form OINTMENT
Route OPHTHALMIC
Labeler VEDCO INC
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-31
Substance MINERAL OIL; WHITE PETROLATUM
Active strength 150; 850 mg/g; mg/g
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 Vedlube
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINERAL OIL 150 mg/g WHITE PETROLATUM 850 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination T5L8T28FGP Internal UNII lookup B6E5W8RQJ4 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 579996 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 50989-476-98 50989047698 1 TUBE in 1 CARTON (50989-476-98) / 3.5 g in 1 TUBE 1 tube 2026-07-31 No No Current