Pharbetol

Product NDC: 73057-350
11-digit product format: 730570350
Labeler code: 73057
Product ID: 73057-350_2c2a6b82-dd55-8cf9-e063-6294a90a68f7
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen 500mg
Dosage form: TABLET, COATED
Route: ORAL
Labeler: Ulai Health LLC
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-07-08
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73057-350-08	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73057-350-11	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73057-350-08	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73057-350-11	`0efc9e666f02…`	`f202fb6c5f17…`

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: 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
1293942	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
c9d3cee1-531c-439f-ae19-07acd366aad6	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
73057-350-08	2022-01-31	Drug Facts
73057-350-11	2022-01-31	Drug Facts
73057-350-08	2022-01-28	Drug Facts
73057-350-11	2022-01-28	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73057-350-08	Pharbetol	100 in 1 BOTTLE, PLASTIC	TABLET, COATED	100		3
73057-350-11	Pharbetol	1000 in 1 BOTTLE, PLASTIC	TABLET, COATED	1000		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73057-350	PHARBETOL (ACETAMINOPHEN 500MG) TABLET, COATED [ULAI HEALTH LLC]	3	Current NDC, Legacy NDC, 2 package rows	20250122_c9d3cee1-531c-439f-ae19-07acd366aad6.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 27 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acetaminophen Diphenhydramine HCL	ACETAMINOPHEN DIPHENHYDRAMINE HCL	WALGREENS CO.	d92d97a8-0ee3-1206-e053-2a95a90a72a8	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	SAM'S WEST INC	0c8e7095-0806-4501-e063-6394a90a89aa	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen Diphenhydramine HCL	ACETAMINOPHEN DIPHENHYDRAMINE HCL	WALGREEN CO.	b3763182-2428-155a-e053-2995a90ab578	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	WALGREENS	e467b78e-9f23-5563-e053-2a95a90a586e	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen Diphenhydramine HCL	ACETAMINOPHEN DIPHENHYDRAMINE HCL	Walgreens	fd7c3250-35d4-494a-e053-6394a90a2db5	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	CVS PHARMACY, INC	1ddb8a2b-3081-3eda-e063-6294a90ab82b	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	CVS PHARMACY, INC	b1307d52-10e6-46e1-e053-2995a90a03b6	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	CVS PHARMACY, INC	c2c6d6a1-b492-506d-e053-2995a90aac23	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	FAMILY DOLLAR	f8383108-0970-9f1e-e053-6294a90ad38f	2025-12-19	Warnings	Exact identifier application number: M013
ACETAMINOPHEN 500 MG	ACETAMINOPHEN	NUVICARE LLC	591ee107-e953-4982-b75f-13a0afd7c4ae	2025-12-19	Warnings	Exact identifier application number: M013
Nuvicare Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	NUVICARE LLC	3ede0fb6-c089-4253-9878-2b01c39e9c87	2025-12-19	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	NUVICARE LLC	3a4aa3c7-b726-4303-8803-74196fa5637a	2025-12-19	Warnings	Exact identifier application number: M013
ACETAMINOPHEN 500 MG	ACETAMINOPHEN	NUVICARE LLC	95edf7bd-b6a7-4be5-9ad7-8748e7c2d06e	2025-12-19	Warnings	Exact identifier application number: M013
Pain Relief PM	ACETAMINOPHEN, DIPHENHYDRAMINE	NUVICARE LLC	32a5611b-9bf6-4850-a7ff-fa240da04f45	2025-12-19	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	BETTER LIVING BRANDS LLC.	ac0e96d0-746e-fb42-e053-2a95a90a1957	2025-12-18	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	BETTER LIVING BRANDS LLC.	ac0e5dc0-96eb-47b2-e053-2995a90add0e	2025-12-18	Warnings	Exact identifier application number: M013
Acetaminophen Diphenhydramine HCl	ACETAMINOPHEN DIPHENHYDRAMINE HCL	BETTER LIVING BRANDS LLC.	ac0f8d5c-d200-1156-e053-2a95a90aece6	2025-12-18	Warnings	Exact identifier application number: M013
Pain and Fever Childrens	ACETAMINOPHEN	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	e55645ab-66f9-4160-8247-395bc5b02711	2025-12-18	Warnings	Exact identifier application number: M013
Dolex Forte	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Pharmadel LLC	3c2d90fc-130d-476c-e063-6294a90a8c15	2025-12-17	Warnings	Exact identifier application number: M013
CareOne Childrens Acetaminophen	ACETAMINOPHEN	American Sales Company	07bc6632-fabb-427d-81f3-c27c54caa6a0	2025-12-17	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	c9d3cee1-531c-439f-ae19-07acd366aad6	3
1293942	Pharbetol 500 MG Oral Tablet	PSN	c9d3cee1-531c-439f-ae19-07acd366aad6	3
1293942	acetaminophen 500 MG Oral Tablet [Pharbetol]	SBD	c9d3cee1-531c-439f-ae19-07acd366aad6	3
198440	acetaminophen 500 MG Oral Tablet	SCD	c9d3cee1-531c-439f-ae19-07acd366aad6	3
198440	APAP 500 MG Oral Tablet	SY	c9d3cee1-531c-439f-ae19-07acd366aad6	3
1293942	APAP 500 MG Oral Tablet [Pharbetol]	SY	c9d3cee1-531c-439f-ae19-07acd366aad6	3
1293942	Pharbetol 500 MG Oral Tablet	SY	c9d3cee1-531c-439f-ae19-07acd366aad6	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
73057-350-08	73057035008	100 TABLET, COATED in 1 BOTTLE, PLASTIC (73057-350-08)	2019-07-08	0000-00-00	No	No	Current
73057-350-11	73057035011	1000 TABLET, COATED in 1 BOTTLE, PLASTIC (73057-350-11)	2019-07-08	0000-00-00	No	No	Current