Acetaminophen

Product NDC: 0121-1882
11-digit product format: 001211882
Labeler code: 0121
Product ID: 0121-1882_bbd6f65a-a6ec-4c17-935c-ed743c45e2c8
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: SUSPENSION
Route: ORAL
Labeler: PAI Holdings, LLC dba PAI Pharma
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-09-03
Substance: ACETAMINOPHEN
Active strength: 325 mg/10.15mL
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0121-1882	0121-1882-94	D	Discontinued by firm		2026-10-20

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0121-1882	0121-1882-94	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0121-1882	0121-1882-94	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

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: Acetaminophen
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	325 mg/10.15mL

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
307668	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
caf5daea-409e-5dd2-e053-2995a90acb12	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0121-1882-00	Acetaminophen	10 in 1 CASE	SUSPENSION	10	5
0121-1882-00	Acetaminophen	10 in 1 TRAY	SUSPENSION	10	5
0121-1882-11	Acetaminophen	10.15 mL in 1 CUP, UNIT-DOSE	SUSPENSION	10.15	5
0121-1882-94	Acetaminophen	3 in 1 CASE	SUSPENSION	3	5
0121-1882-94	Acetaminophen	10 in 1 TRAY	SUSPENSION	10	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0121-1882-00	ML - Milliliter	0121-1882	915601a4-7a0b-4531-b57f-9d407992a1a5	1	2022-01-06
0121-1882-11	ML - Milliliter	0121-1882	d4a8f39f-9bc5-4087-bad3-a8241fd3d175	1	2022-01-06
0121-1882-94	ML - Milliliter	0121-1882	7d77be84-bdf9-4f87-a1e5-1f4c858b8efb	1	2022-01-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0121-1882	ACETAMINOPHEN SUSPENSION [PAI HOLDINGS, LLC DBA PAI PHARMA]	4	Current NDC, Legacy NDC, 5 package rows	20241114_caf5daea-409e-5dd2-e053-2995a90acb12.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 39 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ULINE Aspirin	ASPIRIN	ULINE	9b2b053c-11e7-8169-e053-2995a90ae336	2025-09-09	Warnings	Exact identifier application number: M013
Green Guard Chewable Aspirin 81 mg	ASPIRIN	Unifirst First Aid Corporaiton	173a53ca-b6ea-2042-e063-6294a90a8437	2025-09-08	Warnings	Exact identifier application number: M013
Medique Products Chewable Low Dose Aspirin	ASPIRIN	Unifirst First Aid Corporation	17009501-674d-c839-e063-6294a90a59fa	2025-09-08	Warnings	Exact identifier application number: M013
Henry Schein Acetaminophen	ACETAMINOPHEN	Henry Schein, Inc.	a56a5ca1-578c-40cd-90cc-cc4c2dfec847	2025-09-08	Warnings	Exact identifier application number: M013
Henry Schein Acetaminophen	ACETAMINOPHEN	Henry Schein, Inc.	f43f72de-ff79-4c7e-bd1e-3f0c4c3872fa	2025-09-08	Warnings	Exact identifier application number: M013
Green Guard Maximum Non-Aspirin	ACETAMINOPHEN	Unifirst First Aid Corporation	30f77d4d-839e-4d96-9f24-0254e6a47b81	2025-09-08	Warnings	Exact identifier application number: M013
Green Guard Extra Strength Pain Relief	ASPIRIN. CAFFEINE	Unifirst First Aid Corporation	e729319a-6a2c-bfe6-e053-2a95a90a4620	2025-09-08	Warnings	Exact identifier application number: M013
Medique APAP	ACETAMINOPHEN	Unifirst First Aid Corporation	04805d9c-d959-4870-a185-48b58a880880	2025-09-08	Warnings	Exact identifier application number: M013
Green Guard Maximum Strength Non-Aspirin	ACETAMINOPHEN	Unifirst First Aid Corporation	f77c9554-d1c2-1682-e053-6294a90ac572	2025-09-08	Warnings	Exact identifier application number: M013
Medique Back Pain Relief	MAGNESIUM SALICYLATE TETRAHYDRATE	Unifirst First Aid Corporation	e5563a0a-776a-83d4-e053-2a95a90a9500	2025-09-08	Warnings	Exact identifier application number: M013
MEDIQUE APAP Extra Strength	ACETAMINOPHEN	Unifirst First Aid Corporation	56822785-d5fb-4869-971e-5de637c2eda8	2025-09-08	Warnings	Exact identifier application number: M013
Medique Medi-Seltzer Pain Relief	ASPIFIN	Unifirst First Aid Corporation	3d593dee-b932-b611-e063-6294a90ad3b7	2025-09-08	Warnings	Exact identifier application number: M013
Medique Extra Strength APAP	ACETAMINOPHEN	Unifirst First Aid Corporation	f77f8ef5-4aa8-fa80-e053-6394a90a70c2	2025-09-08	Warnings	Exact identifier application number: M013
Medique Pain Off	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Unifirst First Aid Corporation	c2d7af6b-f477-2462-e053-2995a90aff0f	2025-09-08	Warnings	Exact identifier application number: M013
Medique Extra Strength Apap	ACETAMINOPHEN	Unifirst First Aid Corporation	14bcbaf9-76b6-f8ba-e063-6294a90a91f6	2025-09-08	Warnings	Exact identifier application number: M013
Crane Safety XS Non-Aspirin	ACETAMINOPHEN 500 MG	Crane Safety LLC	9626b3b2-c8ba-5a58-e053-2995a90a35c8	2025-09-08	Warnings	Exact identifier application number: M013
Thompson Aspirin	ASPIRIN	Thompson	9623d9c6-f241-bf4a-e053-2a95a90a4eb5	2025-09-08	Warnings	Exact identifier application number: M013
Thompson XS Pain Ache	ASPIRIN, CAFFEINE	Thompson Safety	e87c2874-2a95-6839-e053-2a95a90ad14b	2025-09-08	Warnings	Exact identifier application number: M013
Medique at Home APAP	ACETAMINOPHEN	Unifirst First Aid Corporation	b5582e23-5079-1f2b-e053-2a95a90ad800	2025-09-08	Warnings	Exact identifier application number: M013
Thompson Extra Strength Non-Aspirin	ACETAMINOPHEN	Thompson	f837c31f-24e5-a8df-e053-6394a90a0b36	2025-09-08	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
307668	acetaminophen 160 MG in 5 mL Oral Suspension	PSN	caf5daea-409e-5dd2-e053-2995a90acb12	5
307668	acetaminophen 32 MG/ML Oral Suspension	SCD	caf5daea-409e-5dd2-e053-2995a90acb12	5
307668	acetaminophen 160 MG per 5 ML Oral Suspension	SY	caf5daea-409e-5dd2-e053-2995a90acb12	5
307668	acetaminophen 320 MG per 10 ML Oral Suspension	SY	caf5daea-409e-5dd2-e053-2995a90acb12	5
307668	acetaminophen 650 MG per 20.3 ML Oral Suspension	SY	caf5daea-409e-5dd2-e053-2995a90acb12	5
307668	acetaminophen 80 MG per 2.5 ML Oral Suspension	SY	caf5daea-409e-5dd2-e053-2995a90acb12	5
307668	APAP 32 MG/ML Oral Suspension	SY	caf5daea-409e-5dd2-e053-2995a90acb12	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0121-1882-00	00121188200	10 TRAY in 1 CASE (0121-1882-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10.15 mL in 1 CUP, UNIT-DOSE (0121-1882-11)	10 tray	2021-09-03	0000-00-00	No	No	Current
0121-1882-11	00121188211	10.15 mL in 1 CUP, UNIT-DOSE	10.15 ml					Historical
0121-1882-94	00121188294	3 TRAY in 1 CASE (0121-1882-94) > 10 CUP, UNIT-DOSE in 1 TRAY > 10.15 mL in 1 CUP, UNIT-DOSE (0121-1882-11)	3 tray	2021-09-03	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Acetaminophen Oral Suspension	PAI Holdings, LLC dba PAI Pharma \| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma	2025-08-18	HUMAN OTC DRUG LABEL	5