NOTTS - Pain Relief PM

Product NDC
82706-009
Requested package NDC
82706-009-01
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

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
NOTTS - Pain Relief PM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1
DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup
TC2D6JAD40Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1092189Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
e6754f62-e3b2-773f-e053-2a95a90ad36aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
82706-009-012024-02-14NOTTS - Pain Relief PM
82706-009-022024-02-14NOTTS - Pain Relief PM
82706-009-012024-01-30NOTTS - Pain Relief PM
82706-009-022024-01-30NOTTS - Pain Relief PM

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82706-009-01NOTTS - Pain Relief PM24 in 1 BOTTLETABLET249
82706-009-01NOTTS - Pain Relief PM1 in 1 CARTONTABLET19
82706-009-02NOTTS - Pain Relief PM50 in 1 BOTTLETABLET509
82706-009-02NOTTS - Pain Relief PM1 in 1 CARTONTABLET19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82706-009NOTTS - PAIN RELIEF PM (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [VIVUNT PHARMA LLC]9Current NDC, Legacy NDC, 4 package rows20241204_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 38 of 79 · 1,576 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Childrens TYLENOLACETAMINOPHENKenvue Brands LLC79669930-f744-4bb1-8325-b75951489b642025-09-17WarningsExact identifier
application number: M013
Pain Reliever PM Extra StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCLL.N.K. International, Inc.ff199db8-c7ea-4b6e-ad8b-3ceeca883d922025-09-15WarningsExact identifier
application number: M013
Acetaminophen PM Extra StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCLFOODHOLD U.S.A., LLCfdd7ce80-d6be-41b9-affd-d024cf306b502025-09-12WarningsExact identifier
application number: M013
Extra Strength Pain RelieverACETAMINOPHENINGLES MARKETS, INC.3e89240b-0e27-fde4-e063-6394a90a779f2025-09-11WarningsExact identifier
application number: M013
Aspirin 81 mg Low DoseASPIRINHEB926fe7b6-9607-469f-912f-4019891067a92025-09-10WarningsExact identifier
application number: M013
Bayer Genuine AspirinASPIRINUnifirst First Aid Corporation356e4ff4-a7f1-4a50-9b86-2555e232b3002025-09-09WarningsExact identifier
application number: M013
Medique at Home AspirinASPIRINUnifirst First Aid Corporationb5a469c1-9ab4-5bd7-e053-2995a90a86d12025-09-09WarningsExact identifier
application number: M013
Medique Products AspirinASPIRINUnifirst First Aid Corporation9b28fed0-a993-ca72-e053-2995a90ac7fd2025-09-09WarningsExact identifier
application number: M013
Unishield AspirinASPIRINUnishieldba106b20-32ac-df90-e053-2995a90adaef2025-09-09WarningsExact identifier
application number: M013
Medi First Pain AcheASPIRIN,CAFFEINEUnifirst First Aid Corporatione82d02d5-3e44-a8f8-e053-2a95a90a26882025-09-09WarningsExact identifier
application number: M013
Medique at Home Back Pain ReliefMAGNESIUM SALICYLATEUnifirst First Aid Corporatione56c4aef-fa0b-74db-e053-2a95a90a97452025-09-09WarningsExact identifier
application number: M013
Travel Savvy AspirinASPIRINBellegrove Medical Supply, Inc.bae80044-ad7f-3bf5-e053-2995a90a42f92025-09-09WarningsExact identifier
application number: M013
McKesson AspirinASPIRINMcKesson Medical-Surgicaldabd741e-e11c-52c1-e053-2a95a90a91d52025-09-09WarningsExact identifier
application number: M013
Travel Savvy Non-AspirinACETAMINOPHEN 325MGBellegrove Medical Supply, Inc.6ab08633-5d5a-42b2-e053-2991aa0ab41a2025-09-09WarningsExact identifier
application number: M013
Direct Safety Aspirin FreeACETAMINOPHENConney Safety Products, LLC1c7369ea-46b6-407c-aa4b-048eb72ff03f2025-09-09WarningsExact identifier
application number: M013
Direct Safety Extra Strength Aspirin FreeACETAMINOPHENConney Safety Products, LLCa524c36a-38f3-4266-8f45-589e194003282025-09-09WarningsExact identifier
application number: M013
Direct Safety AspirinASPIRINDirect Safetyba9ba697-d3df-49d7-e053-2a95a90af4062025-09-09WarningsExact identifier
application number: M013
McKesson Acetaminophen 325ACETAMINOPHENMcKesson Medical-Surgical, Inc.bc2daba5-ce8b-bbda-e053-2a95a90a6f332025-09-09WarningsExact identifier
application number: M013
Uline Acetaminophen Extra StrengthACETAMINOPHENUline90167594-0a49-2492-e053-2a95a90a14012025-09-09WarningsExact identifier
application number: M013
ULINE AspirinASPIRINULINE9b2b053c-11e7-8169-e053-2995a90ae3362025-09-09WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1092189acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral TabletPSNe6754f62-e3b2-773f-e053-2a95a90ad36a9
1092189acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral TabletSCDe6754f62-e3b2-773f-e053-2a95a90ad36a9
1092189APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral TabletSYe6754f62-e3b2-773f-e053-2a95a90ad36a9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82706-009-01827060009011 BOTTLE in 1 CARTON (82706-009-01) / 24 TABLET in 1 BOTTLE1 bottle2022-08-170000-00-00NoNoCurrent