FDA.reportPublic FDA data

All Day Pain Relief

Product NDC
0363-0368
11-digit product format
003630368
Labeler code
0363
Product ID
0363-0368_889efbbf-10a8-4b8b-b9cb-d8eca7b839c7
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Walgreen Company
Application
ANDA074661
Marketing category
ANDA
Marketing start
1997-01-14
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0368-37All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-37All Day Pain Relief270 in 1 BOTTLETABLET, FILM COATED27012
0363-0368-52All Day Pain Relief10 in 1 VIALTABLET, FILM COATED1012
0363-0368-61All Day Pain Relief600 in 1 BOTTLETABLET, FILM COATED60012
0363-0368-62All Day Pain Relief24 in 1 BOTTLETABLET, FILM COATED2412
0363-0368-62All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-71All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-71All Day Pain Relief50 in 1 BOTTLETABLET, FILM COATED5012
0363-0368-75All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-75All Day Pain Relief90 in 1 BOTTLETABLET, FILM COATED9012
0363-0368-76All Day Pain Relief120 in 1 BOTTLETABLET, FILM COATED12012
0363-0368-76All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-78All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-78All Day Pain Relief100 in 1 BOTTLETABLET, FILM COATED10012
0363-0368-79All Day Pain Relief400 in 1 BOTTLETABLET, FILM COATED40012
0363-0368-82All Day Pain Relief1 in 1 CARTONTABLET, FILM COATED112
0363-0368-82All Day Pain Relief200 in 1 BOTTLETABLET, FILM COATED20012

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0368-37EA - Each0363-03680acc0158-7952-4f62-9c62-cb002da432fb12019-08-06
0363-0368-52EA - Each0363-03680db833ae-a454-4d4c-bfe9-d0601882816912013-02-13
0363-0368-61EA - Each0363-03681cbacdd7-0493-4622-b4c4-f98b57d41a7812015-09-10
0363-0368-62EA - Each0363-0368c024da2d-8b9a-43ad-9a7b-90615e682a4c12012-07-24
0363-0368-71EA - Each0363-0368508c0fb0-8658-4c50-a7ff-7d51b8aa866012012-07-24
0363-0368-78EA - Each0363-0368edec4ce7-fca7-449c-9b30-732421114ef312012-07-24
0363-0368-79EA - Each0363-036843fb7953-349c-4cab-a320-33e21d81f54b12013-02-13
0363-0368-82EA - Each0363-0368fe0c9f63-b692-4dd8-9218-0c5ea6ea59fb12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NAPROXEN SODIUMACTIVE INGREDIENT9TN87S3A3CALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
NAPROXENACTIVE MOIETY57Y76R9ATQALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
POVIDONESINACTIVE INGREDIENTFZ989GH94EALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
TALCINACTIVE INGREDIENT7SEV7J4R1UALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0368ALL DAY PAIN RELIEF (NAPROXEN SODIUM) TABLET, FILM COATED [WALGREEN COMPANY]12Current NDC, Legacy NDC, 17 package rows20250114_318d4e2a-7108-4e88-8e56-5bec17ca4a3e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
849574naproxen sodium 220 MG Oral TabletPSN318d4e2a-7108-4e88-8e56-5bec17ca4a3e12
849574naproxen sodium 220 MG Oral TabletSCD318d4e2a-7108-4e88-8e56-5bec17ca4a3e12
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSY318d4e2a-7108-4e88-8e56-5bec17ca4a3e12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-0368-37003630368371 BOTTLE in 1 CARTON (0363-0368-37) > 270 TABLET, FILM COATED in 1 BOTTLE1 bottle2014-07-310000-00-00NoNoCurrent
0363-0368-520036303685210 TABLET, FILM COATED in 1 VIAL (0363-0368-52) 2009-01-210000-00-00NoNoCurrent
0363-0368-6100363036861600 TABLET, FILM COATED in 1 BOTTLE (0363-0368-61) 2011-02-250000-00-00NoNoCurrent
0363-0368-62003630368621 BOTTLE in 1 CARTON (0363-0368-62) > 24 TABLET, FILM COATED in 1 BOTTLE1 bottle1997-01-140000-00-00NoNoCurrent
0363-0368-71003630368711 BOTTLE in 1 CARTON (0363-0368-71) / 50 TABLET, FILM COATED in 1 BOTTLE1 bottle1997-01-140000-00-00NoNoCurrent
0363-0368-75003630368751 BOTTLE in 1 CARTON (0363-0368-75) / 90 TABLET, FILM COATED in 1 BOTTLE1 bottle2022-07-260000-00-00NoNoCurrent
0363-0368-76003630368761 BOTTLE in 1 CARTON (0363-0368-76) / 120 TABLET, FILM COATED in 1 BOTTLE1 bottle2002-07-110000-00-00NoNoCurrent
0363-0368-78003630368781 BOTTLE in 1 CARTON (0363-0368-78) > 100 TABLET, FILM COATED in 1 BOTTLE1 bottle1997-01-140000-00-00NoNoCurrent
0363-0368-7900363036879400 TABLET, FILM COATED in 1 BOTTLE (0363-0368-79) 2010-02-190000-00-00NoNoCurrent
0363-0368-82003630368821 BOTTLE in 1 CARTON (0363-0368-82) > 200 TABLET, FILM COATED in 1 BOTTLE1 bottle2000-05-260000-00-00NoNoCurrent