up and up acetaminophen

Product NDC: 11673-133
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		2026-10-15

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 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 30 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bayer Rapid Relief	ASPIRIN/CAFFEINE ORAL POWDER	Bayer HealthCare LLC.	f1fecbb0-5b55-fe8f-e053-2995a90a0977	2025-12-05	Warnings	Exact identifier application number: M013
Headache Relief, Extra Strength 24/7 Life by 7-Eleven	ACETAMINOPHEN, ASPIRIN, CAFFEINE TABLET, FILM COATED	Lil' Drug Store Products, Inc.	45381b1c-2acd-1524-e063-6394a90a83d9	2025-12-05	Warnings	Exact identifier application number: M013
Acetaminophen Easy Tabs Extra Strength	ACETAMINOPHEN	United Natural Foods, Inc. dba UNFI	729132cd-f209-447a-8949-a90b5a5c01da	2025-12-05	Warnings	Exact identifier application number: M013
Menstrual Pain Relief Complete	ACETAMINOPHEN, PYRILAMINE MALEATE, CAFFEINE	Shield Pharmaceuticals Corp	05fda811-d65f-41b2-89e4-297cdddb3d99	2025-12-05	Warnings	Exact identifier application number: M013
aspirin	ASPIRIN	Health Pharma USA, LLC	3165b0a3-556b-6abe-e063-6394a90a7682	2025-12-04	Warnings	Exact identifier application number: M013
Bayer Genuine Aspirin	ASPIRIN	Bayer HealthCare LLC.	44a08904-68b9-4d06-a28d-21aae3d6140c	2025-12-04	Warnings	Exact identifier application number: M013
Extra Strength Acetaminophen	ACETAMINOPHEN	Geri-Care Pharmaceutical Corp	7a29dde6-a177-6206-e053-2991aa0a01f2	2025-12-04	Warnings	Exact identifier application number: M013
Extra Strength Pain Relief	ACETAMINOPHEN	Geri-Care Pharmaceutical Corp	7570aaa2-3238-4cd3-b788-915caa970dba	2025-12-04	Warnings	Exact identifier application number: M013
Bayer Headache	ASPIRIN AND CAFFEINE	Bayer HealthCare LLC.	c0a92873-0914-6a86-e053-2995a90ac41c	2025-12-04	Warnings	Exact identifier application number: M013
Alka-Seltzer Original Flavor	ALKA-SELTZER ORIGINAL FLAVOR	Bayer HealthCare LLC.	07478020-5ba0-3b67-e054-00144ff88e88	2025-12-04	Warnings	Exact identifier application number: M013
Alka-Seltzer Plus Severe Sinus Cold and Cough Liquid Gels	ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE	Bayer HealthCare LLC.	0dba1329-5b0d-5688-e054-00144ff8d46c	2025-12-04	Warnings	Exact identifier application number: M013
Alka-Seltzer Plus Cold Medicine Sparkling Original	ASPIRIN, CHLORPHENIRAMINE MALEATE, AND PHENYLEPHRINE BITARTRATE	Bayer HealthCare LLC.	78537dcf-b157-4b67-a8b2-5cb144815166	2025-12-04	Warnings	Exact identifier application number: M013
BAYER Aspirin Extra Strength Caplets	BAYER ASPIRIN EXTRA STRENGTH	Bayer HealthCare LLC.	0ae64cdb-4ea0-23af-e054-00144ff88e88	2025-12-04	Warnings	Exact identifier application number: M013
Bayer Chewable - Aspirin Regimen Low Dose Aspirin Cherry Flavored	ASPIRIN	Bayer HealthCare LLC.	070d5713-e018-2913-e054-00144ff8d46c	2025-12-04	Warnings	Exact identifier application number: M013
Bayer Low Dose	ASPIRIN	Bayer HealthCare LLC.	075b103e-0bb4-4b7a-ac0e-5645bcbd0a07	2025-12-04	Warnings	Exact identifier application number: M013
Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, AND SODIUM BICARBONATE	Bayer HealthCare LLC.	5be36a7f-7d1f-468d-9c29-92c8cd3ef1bc	2025-12-04	Warnings	Exact identifier application number: M013
Bayer Aspirin Regimen enteric coated	ASPIRIN	Bayer HealthCare LLC.	0c6ae05f-7634-34d1-e054-00144ff88e88	2025-12-04	Warnings	Exact identifier application number: M013
aspirin pain relief	ASPIRIN	Rite Aid Corporation	ae9d9977-7576-4894-8a32-454828abec9a	2025-12-04	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	RMT HEALTH LLC	2bacffd1-4870-73af-e063-6294a90a19c8	2025-12-02	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN, ASPIRIN AND CAFFEINE	Rite Aid Corporation	d9caee45-be43-45ec-927f-e7fec5c14f07	2025-12-02	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
11673-133-16	11673013316	1 BOTTLE in 1 CARTON (11673-133-16) / 59 mL in 1 BOTTLE	1 bottle	2015-04-22	0000-00-00	No	No	Current
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