up and up acetaminophen

Product NDC: 11673-133
Requested package NDC: 11673-133-26
11-digit product format: 116730133
Labeler code: 11673
Product ID: 11673-133_af4a4454-2cfd-4d5a-93ce-54c0437ccb62
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: SUSPENSION
Route: ORAL
Labeler: Target Corporation
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2015-04-22
Substance: ACETAMINOPHEN
Active strength: 160 mg/5mL
NDC exclude flag: No
Listing certified through: 2027-12-31
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	11673-133	11673-133-26	D	Discontinued by firm		2026-08-17

Additional Listing Data#

Finished product: Yes
Brand name base: up and up acetaminophen
Brand name suffix: infants
Listing expiration: 2027-12-31

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
c1dd8330-fb6b-4d1f-9484-c199dc69214d	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11673-133-16	up and up acetaminopheninfants	59 mL in 1 BOTTLE	SUSPENSION	59	4
11673-133-16	up and up acetaminopheninfants	1 in 1 CARTON	SUSPENSION	1	4
11673-133-26	up and up acetaminopheninfants	1 in 1 CARTON	SUSPENSION	1	4
11673-133-26	up and up acetaminopheninfants	118 mL in 1 BOTTLE	SUSPENSION	118	4

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
ANHYDROUS CITRIC ACID	INACTIVE INGREDIENT	XF417D3PSL	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
CALCIUM SULFATE	INACTIVE INGREDIENT	WAT0DDB505	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
CARBOXYMETHYLCELLULOSE SODIUM	INACTIVE INGREDIENT	K679OBS311	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
CARRAGEENAN	INACTIVE INGREDIENT	5C69YCD2YJ	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
SODIUM PHOSPHATE, TRIBASIC	INACTIVE INGREDIENT	A752Q30A6X	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
SUCRALOSE	INACTIVE INGREDIENT	96K6UQ3ZD4	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11673-133	UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]	3	Current NDC, Legacy NDC, 4 package rows	20240726_c1dd8330-fb6b-4d1f-9484-c199dc69214d.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 1 of 85 · 1,689 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Childrens Pain plus Fever Relief	ACETAMINOPHEN	CVS PHARMACY	e4cbfb06-d826-4d08-95d6-60305c417625	2026-08-14	Warnings	Exact identifier application number: M013
Childrens Pain Relief	ACETAMINOPHEN	CVS Pharmacy,Inc.	3738d35c-1e83-40df-9292-c54e6b2c8353	2026-08-14	Warnings	Exact identifier application number: M013
CVS Childrens Pain plus Fever Relief	ACETAMINOPHEN	CVS PHARMACY	22a48a33-995b-481e-9e4e-1ad7ec346f44	2026-08-14	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	Topco Associates, LLC	8b9e90da-98e2-4d8d-bf6e-54b0a8f8d101	2026-08-12	Warnings	Exact identifier application number: M013
Aspirin 81mg	ASPIRIN	HARRIS TEETER	54e69d5a-55d7-4ebe-8494-0be93613f1e2	2026-08-12	Warnings	Exact identifier application number: M013
Chewable Aspirin	ASPIRIN	HARRIS TEETER	c6a28c83-60c9-3304-e053-2a95a90aa06c	2026-08-12	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	HARRIS TEETER	93cbd3cb-1072-89e6-e053-2995a90a2f15	2026-08-12	Warnings	Exact identifier application number: M013
Adult Chewable Aspirin	ASPIRIN	HARRIS TEETER	c6a28617-1769-7a7d-e053-2995a90a1ea0	2026-08-12	Warnings	Exact identifier application number: M013
Gencare- Pain Relief Acetaminophen	ACETAMINOPHEN	Pioneer Life Sciences, LLC	2111c91b-2fd7-4ab3-946a-d4e0cf46399a	2026-08-12	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	Salado Sales, Inc.	1dbd8480-5cb4-4577-9091-b2a2add4f1af	2026-08-12	Warnings	Exact identifier application number: M013
pain relief childrens	ACETAMINOPHEN	Rite Aid Corporation	29ecdd2d-aeaf-40a8-a347-011088009ea6	2026-08-11	Warnings	Exact identifier application number: M013
Fast Acting Pedia Crae	ACETAMINOPHEN	Randob Labs., Ltd.	e069060f-fbb2-4c7a-b872-00b3ab86d01b	2026-08-11	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	Amazon.com Services LLC	c7cc0681-4c0b-4565-99df-d0168c8ba1ba	2026-08-10	Warnings	Exact identifier application number: M013
GenCare Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Pioneer Life Sciences, LLC	ac8c4bdf-30c9-2b09-e053-2a95a90a9b67	2026-08-09	Warnings	Exact identifier application number: M013
Gencare-Aspirin Low Dose Pain reliever (NSAID)	ASPIRIN	Pioneer Life Sciences, LLC	24d4f46a-c7a5-4e94-804f-1e307d8e8cfc	2026-08-09	Warnings	Exact identifier application number: M013
Aspirin 81 mg	ASPIRIN	DOLGENCORP, LLC	b4064039-2345-4227-b83d-54dc13a838d3	2026-08-07	Warnings	Exact identifier application number: M013
berkley and jensen acetaminophen	ACETAMINOPHEN	BJWC	dee57d73-73ac-48bb-b1da-9971f1ff21c4	2026-08-07	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	P & L Development, LLC	4cd74cec-a209-4e92-b853-fbe5c95f7678	2026-08-06	Warnings	Exact identifier application number: M013
Tension Headache Aspirin-Free	ACETAMINOPHEN, CAFFEINE	Rite Aid Corporation	093a7c26-f2b1-4416-b193-81133d247d2e	2026-08-06	Warnings	Exact identifier application number: M013
ACETAMINOPHEN	ACETAMINOPHEN	Kroger Company	bc17b2e5-4828-6a2e-e053-2995a90a8c63	2026-08-05	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	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4
307668	acetaminophen 32 MG/ML Oral Suspension	SCD	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4
307668	acetaminophen 160 MG per 5 ML Oral Suspension	SY	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4
307668	acetaminophen 320 MG per 10 ML Oral Suspension	SY	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4
307668	acetaminophen 650 MG per 20.3 ML Oral Suspension	SY	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4
307668	acetaminophen 80 MG per 2.5 ML Oral Suspension	SY	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4
307668	APAP 32 MG/ML Oral Suspension	SY	c1dd8330-fb6b-4d1f-9484-c199dc69214d	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11673-133-26	11673013326	1 BOTTLE in 1 CARTON (11673-133-26) > 118 mL in 1 BOTTLE	1 bottle	2018-02-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Target Corporation Infants’ Acetaminophen 160 mg / 5 mL Drug Facts	Target Corporation	2026-05-07	HUMAN OTC DRUG LABEL	4