Home NDC 59390-198 Altalube
Product NDC 59390-198
11-digit product format 593900198
Labeler code 59390
Product ID 59390-198_0c0e9c0d-6205-e63b-e063-6294a90ac0d9
Type HUMAN OTC DRUG
Nonproprietary name Mineral oil and petrolatum
Dosage form OINTMENT
Route OPHTHALMIC
Labeler Altaire Pharmaceuticals Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2002-02-01
Substance MINERAL OIL; PETROLATUM
Active strength 150; 850 mg/g; mg/g
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 Altalube
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINERAL OIL 150 mg/g 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 4T6H12BN9U Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 579996 Internal RxNorm lookup 1088146 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 59390-198-50 Altalube 1 in 1 CARTON OINTMENT 1 4 59390-198-50 Altalube 3.5 g in 1 TUBE OINTMENT 3.5 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59390-198 ALTALUBE (MINERAL OIL AND PETROLATUM) OINTMENT [ALTAIRE PHARMACEUTICALS INC.] 4 Current NDC, Legacy NDC, 2 package rows 20231214_eb65004c-c3a7-4079-bd75-f2857d30c68a.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 Units Marketing start Marketing end Sample Exclude flag Status 59390-198-50 59390019850 1 TUBE in 1 CARTON (59390-198-50) / 3.5 g in 1 TUBE 1 tube 2002-02-01 0000-00-00 No No Current