Home NDC 82706-009 NOTTS - Pain Relief PM
Product NDC 82706-009
11-digit product format 827060009
Labeler code 82706
Product ID 82706-009_284f426f-6cb5-4e7e-e063-6294a90a946e
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Diphenhydramine hydrochloride
Dosage form TABLET
Route ORAL
Labeler VIVUNT PHARMA LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-08-17
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
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base NOTTS - Pain Relief PM
Listing expiration 2026-12-31 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# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82706-009-01 NOTTS - Pain Relief PM 24 in 1 BOTTLE TABLET 24 9 82706-009-01 NOTTS - Pain Relief PM 1 in 1 CARTON TABLET 1 9 82706-009-02 NOTTS - Pain Relief PM 50 in 1 BOTTLE TABLET 50 9 82706-009-02 NOTTS - Pain Relief PM 1 in 1 CARTON TABLET 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82706-009 NOTTS - PAIN RELIEF PM (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [VIVUNT PHARMA LLC] 9 Current NDC, Legacy NDC, 4 package rows 20241204_e6754f62-e3b2-773f-e053-2a95a90ad36a.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 84 · 1,678 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 82706-009-01 82706000901 1 BOTTLE in 1 CARTON (82706-009-01) / 24 TABLET in 1 BOTTLE 1 bottle 2022-08-17 0000-00-00 No No Current 82706-009-02 82706000902 1 BOTTLE in 1 CARTON (82706-009-02) / 50 TABLET in 1 BOTTLE 1 bottle 2022-08-17 0000-00-00 No No Current