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		2026-10-20

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 · 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 59 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pain Relief Regular Strength	ACETAMINOPHEN	MARC GLASSMAN, INC.	e21e821c-9694-5db0-e053-2995a90ad034	2024-10-22	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	MARC GLASSMAN, INC.	e21e90e8-b9f1-1133-e053-2995a90a664b	2024-10-22	Warnings	Exact identifier application number: M013
aspirin	ASPIRIN	Publix Super Markets Inc	c51dae48-aa49-4926-b04a-0da264e08dfa	2024-10-22	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	KROGER COMPANY	b96a2280-ec4f-7c61-e053-2995a90a18bb	2024-10-22	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	HEB	f17a18b0-a7c2-4c64-868c-460cf34e1f7d	2024-10-21	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	HEB	0863aeaa-15ec-4c67-ba79-4dad54555bd2	2024-10-21	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	American Health Packaging	3c0175a0-175b-48b8-9192-3f869690c0f2	2024-10-21	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	American Health Packaging	0d6553bd-3e18-4624-a83a-899bcafb3272	2024-10-21	Warnings	Exact identifier application number: M013
Childrens Acetaminophen Oral Suspension	ACETAMINOPHEN	American Health Packaging	8231dd91-e9e6-4350-a485-fa95d65a6d25	2024-10-21	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	KROGER COMPANY	cf63c372-acdd-6e6e-e053-2995a90a1662	2024-10-21	Warnings	Exact identifier application number: M013
good sense pain relief	ACETAMINOPHEN	L. Perrigo Company	8b56bfc0-2253-458d-99a6-0b0f9ae0ba50	2024-10-21	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	GOODSENSE	662a2bc6-9507-465c-b467-7ae1b2e1dedc	2024-10-18	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	GoodSense	da4339c0-1822-41d8-8c20-214c379a5aa7	2024-10-18	Warnings	Exact identifier application number: M013
Pain Relief PM Extra Strength	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	GoodSense	8972d95a-51da-40b5-8ef1-9dfed220d7eb	2024-10-18	Warnings	Exact identifier application number: M013
Pain Relief Regular Strength	ACETAMINOPHEN	AmeriSource Bergen	d571f520-a56e-4f7f-9214-d89197f742b6	2024-10-18	Warnings	Exact identifier application number: M013
LOW DOSE ASPIRIN	ASPIRIN	Bryant Ranch Prepack	6b4b7f72-dac8-4b59-a58c-7c59d4b1ef32	2024-10-18	Warnings	Exact identifier application number: M013
dg health pain relief	ACETAMINOPHEN	Dolgencorp Inc	2e1470f5-e88f-4d1d-a308-170f7080387e	2024-10-17	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	DISCOUNT DRUG MART	146c735b-5081-4de4-9025-d939d560bbba	2024-10-17	Warnings	Exact identifier application number: M013
Chewable Aspirin	ASPIRIN	DISCOUNT DRUG MART	c8483d64-874c-3056-e053-2995a90ad8aa	2024-10-17	Warnings	Exact identifier application number: M013
Adult Chewable Aspirin	ASPIRIN	DISCOUNT DRUG MART	c8484998-e0e1-ffce-e053-2995a90aa7de	2024-10-17	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
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