FDA.reportPublic FDA data

All Day Pain Relief

Product NDC
59726-169
11-digit product format
597260169
Labeler code
59726
Product ID
59726-169_4f58c6a0-3f3c-42b6-a35b-d0d31c574ec8
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen sodium
Dosage form
TABLET
Route
ORAL
Labeler
P & L Development, LLC
Application
ANDA079096
Marketing category
ANDA
Marketing start
2014-02-28
Substance
NAPROXEN SODIUM
Active strength
220 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
All Day Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NAPROXEN SODIUM220 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9TN87S3A3C
Rxcui849574

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fef6ad89-235f-4274-ba49-a8e53642473eProduct name220250225
87fed3e6-8fba-48ef-96b0-3a7fb54b96ffProduct name320230306
b5fdaaec-7251-4da6-9cb2-4e9e76939ec8Product name120200623
e76dbbc1-775d-722c-08ff-ed45e8a80defProduct name320181002
6f4f4521-fd56-1ae6-888b-3b021bd75c7cProduct name120140508
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59726-169-152022-02-08C16284748780-1d6a99b39-d2c0-a426-e053-dadaa90af4c2Drug Facts
59726-169-152022-01-28C16284748780-1d6a99b39-d2c0-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59726-169-15All Day Pain Relief15 in 1 BOTTLE, PLASTICTABLET155
59726-169-15All Day Pain Relief1 in 1 BOXTABLET15
59726-169-40All Day Pain Relief1 in 1 BOXTABLET15
59726-169-40All Day Pain Relief40 in 1 BOTTLE, PLASTICTABLET405

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NAPROXEN SODIUMACTIVE INGREDIENT9TN87S3A3CALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
NAPROXENACTIVE MOIETY57Y76R9ATQALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
POLYVINYL ALCOHOLINACTIVE INGREDIENT532B59J990ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
POVIDONESINACTIVE INGREDIENTFZ989GH94EALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
TALCINACTIVE INGREDIENT7SEV7J4R1UALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P AND L DEVELOPMENT OF NEW YORK CORPORATION (READYINCASE)]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59726-169ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET [P & L DEVELOPMENT, LLC]5Current NDC, Legacy NDC, 4 package rows20220209_7360ae72-3714-402b-96f1-64dc056bafb8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSN7360ae72-3714-402b-96f1-64dc056bafb85
849574naproxen sodium 220 MG Oral TabletSCD7360ae72-3714-402b-96f1-64dc056bafb85
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSY7360ae72-3714-402b-96f1-64dc056bafb85

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
59726-169-15597260169151 BOTTLE, PLASTIC in 1 BOX (59726-169-15) / 15 TABLET in 1 BOTTLE, PLASTIC2014-02-280000-00-00NoNoCurrent
59726-169-40597260169401 BOTTLE, PLASTIC in 1 BOX (59726-169-40) / 40 TABLET in 1 BOTTLE, PLASTIC2014-02-280000-00-00NoNoCurrent