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 4 of 25 · 494 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SODIUM CHLORIDE 1 GRAM SODIUM CHLORIDE Gendose Pharmaceuticals, LLC ce988ae5-61c6-4324-90e1-a94c8a54d0d0 2026-04-13 Warnings Exact identifier application number: M018 Artificial Tears Lubricant Eye Drops GLYCERIN, PROPYLENE GLYCOL CVS Pharmacy 28297fee-8185-4869-8f39-5bfbf8bf8bfd 2026-04-13 Warnings Exact identifier application number: M018 blink boost GLYCERIN Bausch & Lomb Incorporated e765c224-1718-488f-99b2-976eb60c1d63 2026-04-13 Warnings Exact identifier application number: M018 Retaine Ultra PF POLYETHYLENE GLYCOL OCuSOFT LLC a5aaaf06-772d-44d3-8601-f978ddc48ad7 2026-04-13 Warnings Exact identifier application number: M018 Exovisse Preservative-Free Artificial Tears LUBRICANT EYE GEL DROPS YD BIO USA, INC. 4f20191a-9124-2525-e063-6294a90a8428 2026-04-10 Warnings Exact identifier application number: M018 WE FRESH Lubricating Eye Drops GLYCERIN Oculus Surgical, Inc. 4f253b5d-001b-091e-e063-6394a90a9d39 2026-04-09 Warnings Exact identifier application number: M018 FreshKote Preservative Free Lubricant Eye Drops POVIDONE, POLYVINYL ALCOHOL Eyevance Pharmaceuticals f51c50c3-43ae-4169-9d2b-22b239461dd1 2026-04-08 Warnings Exact identifier application number: M018 Walgreens Sodium Chloride Ophthalmic 5 Percent Hypertonicity Eye SODIUM CHLORIDE Walgreen Company bda3b9db-5fc4-408c-a5ae-d1eeb3ee308d 2026-04-06 Warnings Exact identifier application number: M018 LensMate Preservative-Free Artificial Tears LUBRICANT EYE DROPS YD BIO USA, INC. 4ebacb2b-9b2d-6bc1-e063-6294a90a3426 2026-04-05 Warnings Exact identifier application number: M018 Exovisse Preservative-Free Artificial Tears LUBRICANT EYE GEL DROPS YD BIO USA, INC. 4ebc154b-128b-9dde-e063-6294a90ae00e 2026-04-05 Warnings Exact identifier application number: M018 Sodium Chloride Ophthalmic 5 Percent Hypertonicity Eye SODIUM CHLORIDE Hanlim 4ee80e16-1bb1-8238-e063-6294a90aa719 2026-04-04 Warnings Exact identifier application number: M018 Redness Relief GLYCERIN, NAPHAZOLINE HCL Pharmadel LLC 4c113bb9-814f-d92d-e063-6294a90a8302 2026-03-30 Warnings Exact identifier application number: M018 Moisture Oyster GLYCERIN Moisture Oyster Inc 4e45317a-437f-4d88-e063-6294a90a98d0 2026-03-30 Warnings Exact identifier application number: M018 Crocodile Tears Lubricant Eye Drops GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 Crocodile Tears LLC 4df29336-ea0c-0484-e063-6294a90a685a 2026-03-26 Warnings Exact identifier application number: M018 Artificial Tears Lubricant Eye Drops GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 KC Pharmaceuticals, Inc 4de5c844-85ca-ff9f-e063-6394a90ac12c 2026-03-25 Warnings Exact identifier application number: M018 NOVEHA NIGHTTIME WHITE PETROLATUM Bullet Point LLC 4da24578-e98b-8ce1-e063-6294a90a8bf6 2026-03-24 Warnings Exact identifier application number: M018 BLINK TRIPLE CARE POLYETHYLENE GLYCOL 400 Bausch & Lomb Incorporated a2b34eb0-001b-4f42-a8cc-c2a0150fafcc 2026-03-20 Warnings Exact identifier application number: M018 SODIUM CHLORIDE HYPERTONICITY SODIUM CHLORIDE YYBA CORP 439653b9-99b8-4799-8d67-4a2ada9c6783 2026-03-20 Warnings Exact identifier application number: M018 Altachlore Sodium Chloride Hypertonicity Ophthalmic 5 Percent SODIUM CHLORIDE Altaire Pharmaceuticals Inc. e13fd053-9420-490c-a43e-e14b0930cb4e 2026-03-18 Warnings Exact identifier application number: M018 Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM KC Pharmaceuticals, Inc. 4d1d9b3a-ac5f-db27-e063-6294a90afc3f 2026-03-16 Warnings Exact identifier application number: M018
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