FDA.reportPublic FDA data

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
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage11673-13311673-133-26DDiscontinued by firm2026-10-12

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
IngredientStrength
ACETAMINOPHEN160 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
307668Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
c1dd8330-fb6b-4d1f-9484-c199dc69214dAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-133-16up and up acetaminopheninfants59 mL in 1 BOTTLESUSPENSION594
11673-133-16up and up acetaminopheninfants1 in 1 CARTONSUSPENSION14
11673-133-26up and up acetaminopheninfants1 in 1 CARTONSUSPENSION14
11673-133-26up and up acetaminopheninfants118 mL in 1 BOTTLESUSPENSION1184

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
ACETAMINOPHENACTIVE MOIETY362O9ITL9DUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
CALCIUM SULFATEINACTIVE INGREDIENTWAT0DDB505UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
CARRAGEENANINACTIVE INGREDIENT5C69YCD2YJUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
SODIUM PHOSPHATE, TRIBASICINACTIVE INGREDIENTA752Q30A6XUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
SORBITOLINACTIVE INGREDIENT506T60A25RUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
SUCRALOSEINACTIVE INGREDIENT96K6UQ3ZD4UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1
WATERINACTIVE INGREDIENT059QF0KO0RUP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-133UP AND UP ACETAMINOPHEN INFANTS (ACETAMINOPHEN) SUSPENSION [TARGET CORPORATION]3Current NDC, Legacy NDC, 4 package rows20240726_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 8 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AspirinASPIRINUnited Natural Foods, Inc. dba UNFI19c7f832-d7ec-4dcc-8aa4-f4cbf64c9ff62026-07-02WarningsExact identifier
application number: M013
pain relief EXTRA STRENGTHACETAMINOPHENMeijer Distribution, Inc.ae84eb7e-a70b-4311-b2dc-ad153047a5162026-07-01WarningsExact identifier
application number: M013
Aspirin 325 mgASPIRINHi-Tech Nutraceuticals, LLCb3426a9a-ea99-da30-e053-2995a90a1e4b2026-07-01WarningsExact identifier
application number: M013
Headache Relief Extra StrengthACETAMINOPHEN, ASPIRIN AND CAFFEINESalado Sales, Inc.ca21d576-be3c-495d-9dbd-ed514bf65da72026-07-01WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENMeijer Distribution Inc4e08a7cb-3894-84c3-e063-6394a90a0b422026-06-30WarningsExact identifier
application number: M013
Headache Relief Extra StrengthACETAMINOPHEN, ASPIRIN AND CAFFEINEWal-Mart Stores Inc9b1201af-c802-4e19-b192-bbbf34367db42026-06-30WarningsExact identifier
application number: M013
Pain RelieverACETAMINOPHENP & L Development, LLCfc841cba-8f4f-407b-97de-0422977515bd2026-06-30WarningsExact identifier
application number: M013
Headache ReliefACETAMINOPHEN, ASPIRIN, CAFFEINEUnited Natural Foods, Inc. dba UNFIb6ff2b34-51ee-41bc-8b7d-7520ade0bf362026-06-30WarningsExact identifier
application number: M013
MedlineASPIRINMedline Industries, LP4b0c569a-ed7a-e104-e063-6394a90a6d542026-06-29WarningsExact identifier
application number: M013
Pain Reliever PMACETAMINOPHEN, DIPHENHYDRAMINE HCLWALMART INC.e50b3f60-b827-426c-8e78-8447c89130fe2026-06-29WarningsExact identifier
application number: M013
Acetaminophen PMACETAMINOPHEN, DIPHENHYDRAMINE HCLChain Drug Marketing Association, Inc.e58417f4-3575-4433-ac2e-b7bf9fe8ba102026-06-29WarningsExact identifier
application number: M013
Dr Kids Pain and FeverACETAMINOPHENCalmCo LLC5534a784-a7b1-5599-e063-6294a90a79612026-06-27WarningsExact identifier
application number: M013
TYLENOL Extra StrengthACETAMINOPHENSelect Consumer Group LLC529d3a51-a248-7c02-e063-6294a90a10ae2026-06-27WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENSportpharm LLC830ffcaa-7ff8-4732-bc84-6a8c5e78722d2026-06-25WarningsExact identifier
application number: M013
AspirinASPIRINStrategic Sourcing Services LLCea2ef485-429e-4c63-ba7b-0a6b32892ad22026-06-25WarningsExact identifier
application number: M013
AspirinASPIRINChain Drug Marketing Association, Inc.055d8420-c189-4a9e-acdc-21627935c8eb2026-06-25WarningsExact identifier
application number: M013
AspirinASPIRINTopco Associates, LLC5f32cf74-dbea-496c-ba23-2040ea354f402026-06-25WarningsExact identifier
application number: M013
AspirinASPIRINSalado Sales, Inc.cf3139a5-e36e-48e3-bb6c-e102b0cec5552026-06-25WarningsExact identifier
application number: M013
Pain Relief AspirinASPIRINRite Aid Corporationbd69d3d2-5d38-47c6-98a6-124f7a43b8b02026-06-25WarningsExact identifier
application number: M013
Aspirin Regular StrengthASPIRINWalgreen Company0b27c0fd-7ea8-4588-9169-5ad4e8df77ef2026-06-25WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
307668acetaminophen 160 MG in 5 mL Oral SuspensionPSNc1dd8330-fb6b-4d1f-9484-c199dc69214d4
307668acetaminophen 32 MG/ML Oral SuspensionSCDc1dd8330-fb6b-4d1f-9484-c199dc69214d4
307668acetaminophen 160 MG per 5 ML Oral SuspensionSYc1dd8330-fb6b-4d1f-9484-c199dc69214d4
307668acetaminophen 320 MG per 10 ML Oral SuspensionSYc1dd8330-fb6b-4d1f-9484-c199dc69214d4
307668acetaminophen 650 MG per 20.3 ML Oral SuspensionSYc1dd8330-fb6b-4d1f-9484-c199dc69214d4
307668acetaminophen 80 MG per 2.5 ML Oral SuspensionSYc1dd8330-fb6b-4d1f-9484-c199dc69214d4
307668APAP 32 MG/ML Oral SuspensionSYc1dd8330-fb6b-4d1f-9484-c199dc69214d4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-133-16116730133161 BOTTLE in 1 CARTON (11673-133-16) / 59 mL in 1 BOTTLE1 bottle2015-04-220000-00-00NoNoCurrent
11673-133-26116730133261 BOTTLE in 1 CARTON (11673-133-26) > 118 mL in 1 BOTTLE1 bottle2018-02-150000-00-00NoNoCurrent