Extra Strength Pain Reliever

Product NDC
66715-5680
11-digit product format
667155680
Labeler code
66715
Product ID
66715-5680_2a838f53-0e3d-3892-e063-6394a90a23d6
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen 500 mg, film-coated caplet
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Lil' Drug Store Products, Inc.
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-05-09
Substance
ACETAMINOPHEN
Active strength
500 mg/1
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
Extra Strength Pain Reliever
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198440Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
e5fd2b46-683e-4cf5-e053-2995a90a5512Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66715-5680-4Extra Strength Pain Reliever1 in 1 CARTONTABLET, FILM COATED13
66715-5680-4Extra Strength Pain Reliever50 in 1 BOTTLE, PLASTICTABLET, FILM COATED503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66715-5680EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN 500 MG, FILM-COATED CAPLET) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC.]3Current NDC, Legacy NDC, 2 package rows20250101_e5fd2b46-683e-4cf5-e053-2995a90a5512.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 58 of 79 · 1,576 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetaminophenPAIN RELIEVERMcKesson9d620700-5d00-475f-e053-2995a90a9a3f2024-10-28WarningsExact identifier
application number: M013
Junior Acetaminophen Ages 6-11ACETAMINOPHENChain Drug Consortiumd356bc9c-66f1-45c3-a455-98c0b8890f782024-10-28WarningsExact identifier
application number: M013
leader AcetaminophenACETAMINOPHENCardinal Health 110, LLC. dba Leader36bdcac9-eed4-40f9-a6f2-4c1e773a6b502024-10-25WarningsExact identifier
application number: M013
GOODYS PMACETAMINOPHEN AND DIPHENHYDRAMINE CITRATEMedtech Products Inc.db5d6c2b-688e-4e88-a42d-0fa2b0d8140b2024-10-25WarningsExact identifier
application number: M013
Goodys Extra StrengthACETAMINOPHEN, ASPIRIN, AND CAFFEINEMedtech Products Inc.16d774cc-4247-4bf8-9b5a-c338ffebda3d2024-10-25WarningsExact identifier
application number: M013
aspirinASPIRINPUBLIX SUPER MARKETS INC9e77ab7a-07e8-42aa-e053-2995a90a0d0e2024-10-24WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENKroger Company5bfd9841-c781-43be-b823-d334893ae6ed2024-10-24WarningsExact identifier
application number: M013
Pain ReliefACETAMINOPHENH E Badd6952e-9dd5-487c-93e6-337e9d6a48722024-10-24WarningsExact identifier
application number: M013
Dye Free Pain Reliever ChildrensACETAMINOPHENSafeway, Inc.7d55cb42-295f-473a-941d-71825b44a3c02024-10-24WarningsExact identifier
application number: M013
rapid release pain reliefACETAMINOPHENPublix Super Markets Incd0b34133-d69d-47db-bf51-be942769c6122024-10-24WarningsExact identifier
application number: M013
basic care acetaminophenACETAMINOPHENAmazon.com Services LLC00146b91-008d-4b16-95b0-6077f98821be2024-10-24WarningsExact identifier
application number: M013
equate pain relieverACETAMINOPHENWALMART INC.9a20273e-a4d1-4c38-9efb-e6347f8dc14e2024-10-24WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENMARC GLASSMAN, INC.e221905b-a795-c067-e053-2a95a90a02e72024-10-23WarningsExact identifier
application number: M013
Pain Relief PM Extra StrengthACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEMARC GLASSMAN, INC.e221bbce-83de-0f03-e053-2995a90abca52024-10-23WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENMARC GLASSMAN, INC.e231c2f6-927c-1ab0-e053-2995a90a61212024-10-23WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENMARC GLASSMAN, INC.e23703bb-6087-7985-e053-2995a90aa5ec2024-10-23WarningsExact identifier
application number: M013
Pain Relief PM Extra StrengthACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEMARC GLASSMAN, INC.e237550d-711d-5d87-e053-2995a90affce2024-10-23WarningsExact identifier
application number: M013
AspirinASPIRINHARRIS TEETERa6f15f71-1327-4b71-b9d6-e3e9f02438012024-10-22WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENHARRIS TEETER43308b23-7d4f-4e4f-a497-af71920d86aa2024-10-22WarningsExact identifier
application number: M013
Pain Relief Regular StrengthACETAMINOPHENMARC GLASSMAN, INC.e21e821c-9694-5db0-e053-2995a90ad0342024-10-22WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNe5fd2b46-683e-4cf5-e053-2995a90a55123
198440acetaminophen 500 MG Oral TabletSCDe5fd2b46-683e-4cf5-e053-2995a90a55123
198440APAP 500 MG Oral TabletSYe5fd2b46-683e-4cf5-e053-2995a90a55123

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66715-5680-4667155680041 BOTTLE, PLASTIC in 1 CARTON (66715-5680-4) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2022-05-090000-00-00NoNoCurrent