Pharbetol

Product NDC
71205-990
11-digit product format
712050990
Labeler code
71205
Product ID
71205-990_7429cee4-9642-4421-b4b6-4f942fc4df36
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2006-01-10
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
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
Pharbetol
Listing expiration
2027-12-31

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 SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
9c7d65e4-df2f-47c1-a185-66aaf19aad2bAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71205-990-00Pharbetol100 in 1 BOTTLE, PLASTICTABLET1004
71205-990-11Pharbetol1000 in 1 BOTTLE, PLASTICTABLET10004
71205-990-50Pharbetol50 in 1 BOTTLE, PLASTICTABLET504
71205-990-55Pharbetol500 in 1 BOTTLE, PLASTICTABLET5004

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-990-00EA - Each71205-9901f3fb118-7123-4d07-bcf6-5eea597a352012021-06-02
71205-990-11EA - Each71205-990b6fdcf31-5e5c-40fd-949a-d091d9322ae612021-06-02
71205-990-50EA - Each71205-990f3a2e822-a5a3-4d9b-9642-244d36dfa5cf12021-06-02
71205-990-55EA - Each71205-990630f8edb-00e3-4eb3-9f75-89ca7a9f851012021-06-02

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-990PHARBETOL (ACETAMINOPHEN) TABLET [PROFICIENT RX LP]4Current NDC, Legacy NDC, 4 package rows20240223_9c7d65e4-df2f-47c1-a185-66aaf19aad2b.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 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Good Neighbor Pharmacy Pain ReliefACETAMINOPHENAmerisource Bergen5101125d-4819-4e4b-a0ee-a0ff8d5a0ab12024-10-30WarningsExact identifier
application number: M013
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71205-990-0071205099000100 TABLET in 1 BOTTLE, PLASTIC (71205-990-00) 100 tablet2020-04-010000-00-00NoNoCurrent
71205-990-11712050990111000 TABLET in 1 BOTTLE, PLASTIC (71205-990-11) 1000 tablet2020-04-010000-00-00NoNoCurrent
71205-990-507120509905050 TABLET in 1 BOTTLE, PLASTIC (71205-990-50) 50 tablet2020-04-010000-00-00NoNoCurrent
71205-990-5571205099055500 TABLET in 1 BOTTLE, PLASTIC (71205-990-55) 500 tablet2020-04-010000-00-00NoNoCurrent