Home NDC 0023-0240 REFRESH P.M.
Product NDC 0023-0240
11-digit product format 000230240
Labeler code 0023
Product ID 0023-0240_9e93a73f-478a-40fe-adca-9b1c30bce567
Type HUMAN OTC DRUG
Nonproprietary name mineral oil, petrolatum
Dosage form OINTMENT
Route OPHTHALMIC
Labeler Allergan, Inc.
Application M018
Marketing category OTC MONOGRAPH DRUG
Marketing start 1990-04-23
Substance MINERAL OIL; PETROLATUM
Active strength 425; 573 mg/g; mg/g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 REFRESH P.M.
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINERAL OIL 425 mg/g 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 4T6H12BN9U 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.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0023-0240-04 REFRESH P.M. 1 in 1 CARTON OINTMENT 1 9 0023-0240-04 REFRESH P.M. 3.5 g in 1 TUBE OINTMENT 3.5 9 0023-0240-21 REFRESH P.M. 1 in 1 CARTON OINTMENT 1 9 0023-0240-21 REFRESH P.M. 3.5 g in 1 TUBE OINTMENT 3.5 9
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded mineral oil ACTIVE INGREDIENT T5L8T28FGP REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.] 3 petrolatum ACTIVE INGREDIENT 4T6H12BN9U REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.] 3 mineral oil ACTIVE MOIETY T5L8T28FGP REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.] 3 petrolatum ACTIVE MOIETY 4T6H12BN9U REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.] 3 lanolin alcohols INACTIVE INGREDIENT 884C3FA9HE REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0023-0240 REFRESH P.M. (MINERAL OIL, PETROLATUM) OINTMENT [ALLERGAN, INC.] 8 Current NDC, Legacy NDC, 4 package rows 20240120_24365d64-cd94-41cc-a7e1-033102d98114.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 0023-0240-04 00023024004 1 TUBE in 1 CARTON (0023-0240-04) > 3.5 g in 1 TUBE 1 tube 1990-04-23 0000-00-00 No No Current 0023-0240-21 00023024021 1 TUBE in 1 CARTON (0023-0240-21) > 3.5 g in 1 TUBE 1 tube 1990-04-23 0000-00-00 No No Current