Home NDC 73581-710 Mineral Oil/White Petrolatum
Product NDC 73581-710
11-digit product format 735810710
Labeler code 73581
Product ID 73581-710_5905b300-6f20-a61f-e063-6394a90a1123
Type HUMAN OTC DRUG
Nonproprietary name Mineral Oil/White Petrolatum
Dosage form OINTMENT
Route OPHTHALMIC
Labeler YYBA CORP
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-17
Substance MINERAL OIL; WHITE PETROLATUM
Active strength 425; 573 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 Mineral Oil/White Petrolatum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINERAL OIL 425 mg/g WHITE PETROLATUM 573 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 702008 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 · 499 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 73581-710-01 73581071001 1 TUBE in 1 CARTON (73581-710-01) / 3.5 g in 1 TUBE 1 tube 2026-08-17 No No Current