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		2026-10-16

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 55 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ACETAMINOPHEN (RED)	ACETAMINOPHEN	Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd	a352f588-4a70-42b2-8f9c-a73a0629517d	2024-11-25	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength	ACETAMINOPHEN	Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.	5c42dd28-820c-4cc5-9016-11ad5e580616	2024-11-25	Warnings	Exact identifier application number: M013
equate pain reliever	ACETAMINOPHEN	WALMART INC.	4518fe82-3ba8-4e9e-a036-776df7fb8d57	2024-11-21	Warnings	Exact identifier application number: M013
Family Wellness Pain Reliever	ASPIRIN	FAMILY WELLNESS SERVICES, INC.	075e19f4-1a58-aedd-e063-6294a90af708	2024-11-20	Warnings	Exact identifier application number: M013
Mejoralito	ACETAMINOPHEN	OPMX Chula Vista	fd2ecde0-296e-060f-e053-6294a90afd98	2024-11-15	Warnings	Exact identifier application number: M013
Temp X	ACETAMINOPHEN	OPMX Chula Vista	fd2edc32-0351-c991-e053-6294a90ab4ce	2024-11-15	Warnings	Exact identifier application number: M013
CVS Health Extra Strength Antacid and Pain Reliever	ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE	CVS Pharmacy	afe9e755-18ba-305f-e053-2995a90aa8d0	2024-11-14	Warnings	Exact identifier application number: M013
Walgreens Effervescent Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Walgreens	667418fc-a3ab-cbc7-e053-2a91aa0a2023	2024-11-13	Warnings	Exact identifier application number: M013
Up and Up Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Target Corporation	a72eef45-b985-638a-e053-2995a90aa20a	2024-11-13	Warnings	Exact identifier application number: M013
Signature Care Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Safeway, Inc	6e120024-475a-73af-e053-2a91aa0a42a6	2024-11-13	Warnings, Adverse reactions	Exact identifier application number: M013
Kroger Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Kroger Company	6d858b0e-a3c8-2686-e053-2991aa0acc06	2024-11-13	Warnings	Exact identifier application number: M013
TopCare Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Topco Associates LLC	639f9d57-f26a-708a-e053-2a91aa0a6962	2024-11-13	Warnings, Adverse reactions	Exact identifier application number: M013
Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	H. E. Butt Grocery Company	6418cde9-607b-4ca1-e053-2991aa0a9170	2024-11-13	Warnings	Exact identifier application number: M013
Bromo Seltzer	ASPIRIN, SODIUM BICARBONATE, CITRIC ACID	Tower Laboratories Ltd	8ff88ee1-e33e-4051-992f-24e2720c48ce	2024-11-13	Warnings	Exact identifier application number: M013
Care One Original Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Foodhold U.S.A.	8f662c51-d2fa-6458-e053-2995a90ac6fd	2024-11-13	Warnings	Exact identifier application number: M013
Top Value Effervescent Pain Relief	APIRIN, CITRIC ACID, SODIUM BICARBONATE	Tower Laboratories Ltd	43c7f435-735c-3fab-e054-00144ff88e88	2024-11-13	Warnings, Adverse reactions	Exact identifier application number: M013
DG Health Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	DOLGENCORP, INC	8f1343d5-2884-3a14-e053-2a95a90a2f90	2024-11-13	Warnings	Exact identifier application number: M013
Good Sense Effervescent Antacid and Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Good Sense	cd25b0c3-0134-beef-e053-2a95a90a092b	2024-11-13	Warnings	Exact identifier application number: M013
Drug Mart Effervescent Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Discount Drug Mart, Inc	8bc65603-1dbf-30ab-e053-2995a90a7c15	2024-11-13	Warnings	Exact identifier application number: M013
Best Choice Effervescent Antacid Pain Relief	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE	Valu Merchandisers Company	8aab905b-5fe7-dddb-e053-2995a90a6c6f	2024-11-13	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