Home NDC 59726-868 Pain Reliever PM
Product NDC 59726-868
11-digit product format 597260868
Labeler code 59726
Product ID 59726-868_fd04bd61-2bce-4ec0-99b0-ebd0995d3aba
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen Diphenhydramine HCL
Dosage form TABLET, COATED
Route ORAL
Labeler P & L Development, LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-03-26
Marketing end 2026-12-26
Substance ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 500; 25 mg/1; mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Pain Reliever PM
Brand name suffix extra strength Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1 DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup TC2D6JAD40 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1092189 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59726-868-10 Pain Reliever PMextra strength 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 7 59726-868-10 Pain Reliever PMextra strength 1 in 1 BOX TABLET, COATED 1 7 59726-868-24 Pain Reliever PMextra strength 1 in 1 BOX TABLET, COATED 1 7 59726-868-24 Pain Reliever PMextra strength 24 in 1 BOTTLE, PLASTIC TABLET, COATED 24 7 59726-868-50 Pain Reliever PMextra strength 1 in 1 BOX TABLET, COATED 1 7 59726-868-50 Pain Reliever PMextra strength 50 in 1 BOTTLE, PLASTIC TABLET, COATED 50 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59726-868 PAIN RELIEVER PM EXTRA STRENGTH (ACETAMINOPHEN DIPHENHYDRAMINE HCL) TABLET, COATED [P & L DEVELOPMENT, LLC] 6 Current NDC, Legacy NDC, 6 package rows 20240805_90eba2e8-52c3-43f5-ba93-4a520368c7f4.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 1 of 85 · 1,681 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 59726-868-10 59726086810 1 BOTTLE, PLASTIC in 1 BOX (59726-868-10) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 2021-03-26 2026-12-26 No No Current 59726-868-24 59726086824 1 BOTTLE, PLASTIC in 1 BOX (59726-868-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 2021-03-26 2026-12-26 No No Historical 59726-868-50 59726086850 1 BOTTLE, PLASTIC in 1 BOX (59726-868-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC 2021-03-26 2026-12-26 No No Current