PANADOL

Product NDC: 0135-0609
Requested package NDC: 0135-0609-01
11-digit product format: 001350609
Labeler code: 0135
Product ID: 0135-0609_10c10ae1-2b66-f708-e063-6394a90a0fca
Type: HUMAN OTC DRUG
Nonproprietary name: acetaminophen
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Haleon US Holdings LLC
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2017-03-15
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: PANADOL
Brand name suffix: Extra Strength
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
362O9ITL9D	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198440	Internal RxNorm lookup
200977	Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
0135-0609-01	Drug Facts
0135-0609-02	Drug Facts
0135-0609-03	Drug Facts
0135-0609-04	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0135-0609-01	PANADOLExtra Strength	24 in 1 BOTTLE	TABLET, FILM COATED	24	7
0135-0609-01	PANADOLExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	7
0135-0609-02	PANADOLExtra Strength	50 in 1 BOTTLE	TABLET, FILM COATED	50	7
0135-0609-02	PANADOLExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	7
0135-0609-03	PANADOLExtra Strength	100 in 1 BOTTLE	TABLET, FILM COATED	100	7
0135-0609-03	PANADOLExtra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	7
0135-0609-04	PANADOLExtra Strength	50 in 1 CARTON	TABLET, FILM COATED	50	7
0135-0609-05	PANADOLExtra Strength	2 in 1 PACKET	TABLET, FILM COATED	2	7

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0135-0609-01	EA - Each	0135-0609	fe1f0735-9843-4fe3-bb42-0a2256c3b2c6	1	2022-12-07
0135-0609-02	EA - Each	0135-0609	2e35bea5-0a22-4410-ac97-e2465812c2d8	1	2022-12-07
0135-0609-03	EA - Each	0135-0609	a22d623d-3cc7-4af6-a98a-fbe4fceff390	1	2022-12-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0135-0609	PANADOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [HALEON US HOLDINGS LLC]	7	Current NDC, Legacy NDC, 8 package rows	20240207_b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b.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 57 of 79 · 1,570 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
dg health pain relief	ACETAMINOPHEN	Dolgencorp, LLC	382fa2cc-1c39-4bee-b528-08b11ec945af	2024-11-02	Warnings	Exact identifier application number: M013
acetaminophen	ACETAMINOPHEN	Bryant Ranch Prepack	f7e20527-1d4b-434c-997b-3eb8211fdaa1	2024-11-01	Warnings	Exact identifier application number: M013
Aspirin Enteric Safety Coated	ASPIRIN	Publix Supermarkets, Inc.	a661a9ed-9b31-46b1-aafb-61d1ba8a4918	2024-11-01	Warnings	Exact identifier application number: M013
acetaminophen	ACETAMINOPHEN	Bryant Ranch Prepack	614e69c7-d3cb-4d47-9603-c1c14b87544c	2024-11-01	Warnings	Exact identifier application number: M013
infants fever reducer and pain reliever	ACETAMINOPHEN	Rite Aid Corporation	baee03b8-fcfd-440e-90ea-1ee2a18516ef	2024-11-01	Warnings	Exact identifier application number: M013
good neighbor pharmacy infants pain and fever	ACETAMINOPHEN	Amerisource Bergen	bfb954b7-3a79-4bca-95e8-d39e1074b07f	2024-11-01	Warnings	Exact identifier application number: M013
EXTRA STRENGTH PAIN RELIEVER	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Proficient Rx LP	bf365bfc-35cc-47f9-a50b-ff2b38d7316b	2024-11-01	Warnings	Exact identifier application number: M013
Infants Pain Relief	ACETAMINOPHEN	Publix Super Markets Inc	0bc33897-afc2-4d11-be6c-a26480f448bf	2024-10-31	Warnings	Exact identifier application number: M013
equate infants pain and fever	ACETAMINOPHEN	WALMART INC.	34b2512e-743b-45db-92cb-ea05e2f47b3d	2024-10-31	Warnings	Exact identifier application number: M013
foster and thrive infants pain and fever	ACETAMINOPHEN	Strategic Sourcing Services LLC	45770ad6-9bf7-41bd-a724-e5260cd31fa1	2024-10-31	Warnings	Exact identifier application number: M013
Midol Complete	ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE TABLET	Lil' Drug Store Products, Inc.	d20425a4-f074-4154-e053-2995a90ae9fd	2024-10-30	Warnings	Exact identifier application number: M013
up and up infants acetaminophen	ACETAMINOPHEN	Target Corporation	31104956-04d7-41b5-82be-219ded5c02a9	2024-10-30	Warnings	Exact identifier application number: M013
Sunmark Aspirin	ASPIRIN	Strategic Sourcing Services LLC	a7139686-b351-47dc-a395-832429aaa569	2024-10-30	Warnings	Exact identifier application number: M013
Good Neighbor Pharmacy Pain Relief	ACETAMINOPHEN	Amerisource Bergen	5101125d-4819-4e4b-a0ee-a0ff8d5a0ab1	2024-10-30	Warnings	Exact identifier application number: M013
Acetaminophen	PAIN RELIEVER	McKesson	9d620700-5d00-475f-e053-2995a90a9a3f	2024-10-28	Warnings	Exact identifier application number: M013
Junior Acetaminophen Ages 6-11	ACETAMINOPHEN	Chain Drug Consortium	d356bc9c-66f1-45c3-a455-98c0b8890f78	2024-10-28	Warnings	Exact identifier application number: M013
leader Acetaminophen	ACETAMINOPHEN	Cardinal Health 110, LLC. dba Leader	36bdcac9-eed4-40f9-a6f2-4c1e773a6b50	2024-10-25	Warnings	Exact identifier application number: M013
GOODYS PM	ACETAMINOPHEN AND DIPHENHYDRAMINE CITRATE	Medtech Products Inc.	db5d6c2b-688e-4e88-a42d-0fa2b0d8140b	2024-10-25	Warnings	Exact identifier application number: M013
Goodys Extra Strength	ACETAMINOPHEN, ASPIRIN, AND CAFFEINE	Medtech Products Inc.	16d774cc-4247-4bf8-9b5a-c338ffebda3d	2024-10-25	Warnings	Exact identifier application number: M013
aspirin	ASPIRIN	PUBLIX SUPER MARKETS INC	9e77ab7a-07e8-42aa-e053-2995a90a0d0e	2024-10-24	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
200977	Panadol Extra Strength 500 MG Oral Tablet	PSN	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
200977	acetaminophen 500 MG Oral Tablet [Panadol]	SBD	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
198440	acetaminophen 500 MG Oral Tablet	SCD	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
198440	APAP 500 MG Oral Tablet	SY	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
200977	APAP 500 MG Oral Tablet [Panadol]	SY	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
200977	Panadol 500 MG Oral Tablet	SY	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7
200977	Panadol Extra Strength 500 MG Oral Tablet	SY	b2fe7f47-1a2e-40ee-8f8f-38f2028dce1b	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0135-0609-01	00135060901	1 BOTTLE in 1 CARTON (0135-0609-01) / 24 TABLET, FILM COATED in 1 BOTTLE	1 bottle	2017-03-15	0000-00-00	No	No	Current