All Day Relief

Product NDC
56062-748
11-digit product format
560620748
Labeler code
56062
Product ID
56062-748_581830ee-5c9a-40aa-8bf7-c02dcda51e0f
Type
HUMAN OTC DRUG
Nonproprietary name
Naproxen Sodium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Publix Supermarkets, Inc.
Application
ANDA208363
Marketing category
ANDA
Marketing start
2019-06-30
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 Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NAPROXEN SODIUM220 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9TN87S3A3C
Rxcui1112231

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fef6ad89-235f-4274-ba49-a8e53642473eProduct name220250225
87fed3e6-8fba-48ef-96b0-3a7fb54b96ffProduct name320230306
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
b5fdaaec-7251-4da6-9cb2-4e9e76939ec8Product name120200623
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e76dbbc1-775d-722c-08ff-ed45e8a80defProduct name320181002
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
6f4f4521-fd56-1ae6-888b-3b021bd75c7cProduct name120140508
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
56062-748-402020-11-17C16284748780-1ab0e2407-35f9-f274-e053-dbdaa90a6471Drug Facts
56062-748-402020-09-27C16284748780-1ab0e2407-35f9-f274-e053-dbdaa90a6471Drug Facts
56062-748-402020-09-25C16284748780-1ab0e2407-35f9-f274-e053-dbdaa90a6471Drug Facts
56062-748-402020-07-22C16284748780-1ab0e2407-35f9-f274-e053-dbdaa90a6471Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56062-748-40All Day Relief40 in 1 BOTTLE, PLASTICCAPSULE, LIQUID FILLED405
56062-748-40All Day Relief1 in 1 BOXCAPSULE, LIQUID FILLED15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56062-748ALL DAY RELIEF (NAPROXEN SODIUM) CAPSULE, LIQUID FILLED [PUBLIX SUPERMARKETS, INC.]5Current NDC, Legacy NDC, 2 package rows20240124_4db86c5b-62bb-4638-9f1e-98dc2680d6cc.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1112231naproxen sodium 220 MG Oral CapsulePSN4db86c5b-62bb-4638-9f1e-98dc2680d6cc5
1112231naproxen sodium 220 MG Oral CapsuleSCD4db86c5b-62bb-4638-9f1e-98dc2680d6cc5
1112231naproxen sodium 220 MG (as naproxen 200 MG) Oral CapsuleSY4db86c5b-62bb-4638-9f1e-98dc2680d6cc5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
56062-748-40560620748401 BOTTLE, PLASTIC in 1 BOX (56062-748-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC2019-06-300000-00-00NoNoCurrent