Extra Strength Acetaminophen

Product NDC: 69732-001
Requested package NDC: 69732-001-01
11-digit product format: 697320001
Labeler code: 69732
Product ID: 69732-001_55f92c95-a399-6cf1-e063-6394a90a07af
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: Hi-Tech Nutraceuticals, LLC
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-04-30
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 15 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

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 Acetaminophen
Listing expiration: 2027-12-31

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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198440	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
a36be487-7a36-550f-e053-2a95a90a95c1	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69732-001-01	2023-01-30	C162847	48780-1	f386c64a-30ea-0266-e053-dadaa90a7c1a	a36be487-7a36-550f-e053-2a95a90a95c1
69732-001-01	2023-01-30	C162847	48780-1	f386c64a-30ea-0266-e053-dadaa90a7c1a	a36be487-7a36-550f-e053-2a95a90a95c1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69732-001-01	Extra Strength Acetaminophen	30 in 1 BOTTLE, PLASTIC	TABLET	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69732-001	EXTRA STRENGTH ACETAMINOPHEN (ACETAMINOPHEN) TABLET [HI-TECH NUTRACEUTICALS, LLC]	2	Current NDC, Legacy NDC, 1 package rows	20200430_a36be487-7a36-550f-e053-2a95a90a95c1.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 76 of 79 · 1,570 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acetaminophen	ACETAMINOPHEN	Aurohealth LLC	30756257-f748-4a5d-b031-dd267d0f91ad	2023-11-29	Warnings	Exact identifier application number: M013
Aurophen Regular Strength	ACETAMINOPHEN	Aurohealth LLC	8eda893f-5266-4b7a-95b9-2e194973cf06	2023-11-29	Warnings	Exact identifier application number: M013
Childrens Pain Relief	ACETAMINOPHEN	Aurohealth LLC	00ec6518-b5e3-49d1-a342-139381c3bfd2	2023-11-29	Warnings	Exact identifier application number: M013
CHILDRENS PAIN RELIEF	ACETAMINOPHEN	Better Living Brands, LLC	fadb4c09-071f-56c0-e053-6294a90ae6c1	2023-11-28	Warnings	Exact identifier application number: M013
Acetaminophen and Diphenhydramine hydrochloride	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	Better Living Brands, LLC	fc07d516-9ffe-9989-e053-6294a90ae1a5	2023-11-28	Warnings	Exact identifier application number: M013
NOTTS - Tension Headache	ACETAMINOPHEN, CAFFEINE	VIVUNT PHARMA LLC	08f2ae03-967b-ad7e-e063-6294a90a8484	2023-11-24	Warnings	Exact identifier application number: M013
Sanatos Multi Symptoms Nighttime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Pharmadel LLC	0a60326a-a17b-e843-e063-6394a90ac211	2023-11-22	Warnings	Exact identifier application number: M013
Sanatos Nighttime Multi Symptoms	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Pharmadel LLC	0ab188f3-f7f9-d665-e063-6294a90a198a	2023-11-22	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	TIME CAP LABS INC	fe12519c-3e5f-4592-bd34-2d6b81b981f4	2023-11-22	Warnings	Exact identifier application number: M013
Rugby Regular Strength Acetaminophen	ACETAMINOPHEN	A-S Medication Solutions	400d4a29-9e39-4e74-8272-37be5d789924	2023-11-22	Warnings	Exact identifier application number: M013
RIGHT REMEDIES Pain Relief Extra Strength Caplet	ACETAMINOPHEN	Strive Pharmaceuticals Inc.	dcce28d9-8528-489e-b995-1d98e9d0e6ad	2023-11-21	Warnings	Exact identifier application number: M013
Sanatos Multi Symptom Daytime	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCI	Pharmadel LLC	0ab11691-5b29-55fc-e063-6394a90aa328	2023-11-17	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	A-S Medication Solutions	1e223faa-f6d0-4235-bc4c-6cfca84a5b0a	2023-11-17	Warnings	Exact identifier application number: M013
SanaTos X	ACETAMINOPHEN, DEXTROMETHORPHAN HBR,GUAIFENESIN, PHENYLEPHRINE HCI	Pharmadel LLC	85b8ef3d-7318-7f3b-e053-2991aa0a0777	2023-11-14	Warnings	Exact identifier application number: M013
RIGHT REMEDIES EXTRA STRENGTH PM Pain Relief	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Strive Pharmaceuticals Inc.	8badbaad-eb35-4251-a779-00474819360d	2023-11-13	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Trifecta Pharmaceuticals USA LLC	09935a74-34b0-0e7c-e063-6294a90a7c83	2023-11-07	Warnings	Exact identifier application number: M013
Pain Relief PM	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	AMERIFOODS TRADING COMPANY	f6dd6396-93e9-1096-e053-6394a90af06d	2023-11-02	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	RETAIL BUSINESS SERVICES , LLC.	eb644e9e-36dc-5f84-e053-2a95a90affa5	2023-11-02	Warnings	Exact identifier application number: M013
Good Sense Childrens Pain and Fever	ACETAMINOPHEN	Proficient Rx LP	46527b1f-7515-44ce-b5cb-9d24223b9af1	2023-11-01	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	A-S Medication Solutions	12feb32b-4b8c-4b17-9e86-cb286457b088	2023-11-01	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	a36be487-7a36-550f-e053-2a95a90a95c1	2
198440	acetaminophen 500 MG Oral Tablet	SCD	a36be487-7a36-550f-e053-2a95a90a95c1	2
198440	APAP 500 MG Oral Tablet	SY	a36be487-7a36-550f-e053-2a95a90a95c1	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69732-001-01	69732000101	30 TABLET in 1 BOTTLE, PLASTIC (69732-001-01)	30 tablet	2020-04-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Acetaminophen - Hi-Tech Nutraceuticals, LLC \| Hi-Techn Nutraceutical, LLC	Hi-Tech Nutraceuticals, LLC \| Hi-Techn Nutraceutical, LLC	2026-07-06	HUMAN OTC DRUG LABEL	3
Walgreens 125-Count Extra Strength	Hi-Tech Nutraceuticals, LLC \| Hi-Techn Nutraceutical, LLC	2020-08-30	HUMAN OTC DRUG LABEL	2