Up and Up childrens acetaminophen

Product NDC: 11673-105
11-digit product format: 116730105
Labeler code: 11673
Product ID: 11673-105_9bc7510c-d284-4ca5-8a86-a346f690f3b1
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: SUSPENSION
Route: ORAL
Labeler: Target Corporation
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2009-07-08
Substance: ACETAMINOPHEN
Active strength: 160 mg/5mL
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	11673-105	11673-105-28	D	Discontinued by firm		2026-10-15

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 · 12 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…`

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: Up and Up childrens acetaminophen
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	160 mg/5mL

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
9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11673-105-26	Up and Up childrens acetaminophen	1 in 1 CARTON	SUSPENSION	1	9
11673-105-26	Up and Up childrens acetaminophen	118 mL in 1 BOTTLE	SUSPENSION	118	9
11673-105-28	Up and Up childrens acetaminophen	1 in 1 CARTON	SUSPENSION	1	9
11673-105-28	Up and Up childrens acetaminophen	148 mL in 1 BOTTLE	SUSPENSION	148	9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
11673-105-26	ML - Milliliter	11673-105	95507952-95a6-46dd-a5fe-cecba8536597	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
BUTYLPARABEN	INACTIVE INGREDIENT	3QPI1U3FV8	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
CALCIUM SULFATE	INACTIVE INGREDIENT	WAT0DDB505	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
CARRAGEENAN	INACTIVE INGREDIENT	5C69YCD2YJ	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
D&C RED NO. 33	INACTIVE INGREDIENT	9DBA0SBB0L	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
HIGH FRUCTOSE CORN SYRUP	INACTIVE INGREDIENT	XY6UN3QB6S	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
SODIUM PHOSPHATE, TRIBASIC	INACTIVE INGREDIENT	A752Q30A6X	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
SORBITOL	INACTIVE INGREDIENT	506T60A25R	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-105	UP AND UP CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	9	Current NDC, Legacy NDC, 4 package rows	20240913_9c3ba4dd-f51b-46ce-91b8-8b617c7b78da.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 8 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aspirin	ASPIRIN	United Natural Foods, Inc. dba UNFI	19c7f832-d7ec-4dcc-8aa4-f4cbf64c9ff6	2026-07-02	Warnings	Exact identifier application number: M013
pain relief EXTRA STRENGTH	ACETAMINOPHEN	Meijer Distribution, Inc.	ae84eb7e-a70b-4311-b2dc-ad153047a516	2026-07-01	Warnings	Exact identifier application number: M013
Aspirin 325 mg	ASPIRIN	Hi-Tech Nutraceuticals, LLC	b3426a9a-ea99-da30-e053-2995a90a1e4b	2026-07-01	Warnings	Exact identifier application number: M013
Headache Relief Extra Strength	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Salado Sales, Inc.	ca21d576-be3c-495d-9dbd-ed514bf65da7	2026-07-01	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Meijer Distribution Inc	4e08a7cb-3894-84c3-e063-6394a90a0b42	2026-06-30	Warnings	Exact identifier application number: M013
Headache Relief Extra Strength	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Wal-Mart Stores Inc	9b1201af-c802-4e19-b192-bbbf34367db4	2026-06-30	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	P & L Development, LLC	fc841cba-8f4f-407b-97de-0422977515bd	2026-06-30	Warnings	Exact identifier application number: M013
Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	United Natural Foods, Inc. dba UNFI	b6ff2b34-51ee-41bc-8b7d-7520ade0bf36	2026-06-30	Warnings	Exact identifier application number: M013
Medline	ASPIRIN	Medline Industries, LP	4b0c569a-ed7a-e104-e063-6394a90a6d54	2026-06-29	Warnings	Exact identifier application number: M013
Pain Reliever PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	WALMART INC.	e50b3f60-b827-426c-8e78-8447c89130fe	2026-06-29	Warnings	Exact identifier application number: M013
Acetaminophen PM	ACETAMINOPHEN, DIPHENHYDRAMINE HCL	Chain Drug Marketing Association, Inc.	e58417f4-3575-4433-ac2e-b7bf9fe8ba10	2026-06-29	Warnings	Exact identifier application number: M013
Dr Kids Pain and Fever	ACETAMINOPHEN	CalmCo LLC	5534a784-a7b1-5599-e063-6294a90a7961	2026-06-27	Warnings	Exact identifier application number: M013
TYLENOL Extra Strength	ACETAMINOPHEN	Select Consumer Group LLC	529d3a51-a248-7c02-e063-6294a90a10ae	2026-06-27	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	Sportpharm LLC	830ffcaa-7ff8-4732-bc84-6a8c5e78722d	2026-06-25	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Strategic Sourcing Services LLC	ea2ef485-429e-4c63-ba7b-0a6b32892ad2	2026-06-25	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Chain Drug Marketing Association, Inc.	055d8420-c189-4a9e-acdc-21627935c8eb	2026-06-25	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Topco Associates, LLC	5f32cf74-dbea-496c-ba23-2040ea354f40	2026-06-25	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Salado Sales, Inc.	cf3139a5-e36e-48e3-bb6c-e102b0cec555	2026-06-25	Warnings	Exact identifier application number: M013
Pain Relief Aspirin	ASPIRIN	Rite Aid Corporation	bd69d3d2-5d38-47c6-98a6-124f7a43b8b0	2026-06-25	Warnings	Exact identifier application number: M013
Aspirin Regular Strength	ASPIRIN	Walgreen Company	0b27c0fd-7ea8-4588-9169-5ad4e8df77ef	2026-06-25	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	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9
307668	acetaminophen 32 MG/ML Oral Suspension	SCD	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9
307668	acetaminophen 160 MG per 5 ML Oral Suspension	SY	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9
307668	acetaminophen 320 MG per 10 ML Oral Suspension	SY	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9
307668	acetaminophen 650 MG per 20.3 ML Oral Suspension	SY	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9
307668	acetaminophen 80 MG per 2.5 ML Oral Suspension	SY	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9
307668	APAP 32 MG/ML Oral Suspension	SY	9c3ba4dd-f51b-46ce-91b8-8b617c7b78da	9

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-105-26	11673010526	1 BOTTLE in 1 CARTON (11673-105-26) / 118 mL in 1 BOTTLE	1 bottle	2009-07-08	0000-00-00	No	No	Current
11673-105-28	11673010528	1 BOTTLE in 1 CARTON (11673-105-28) > 148 mL in 1 BOTTLE	1 bottle	2012-08-24	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Target Corporation Children's Acetaminophen Drug Facts	Target Corporation	2024-08-23	HUMAN OTC DRUG LABEL	9