FDA.reportPublic FDA data

NDC 17856-0166-2 - ACETAMINOPHEN

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
17856-0166
Requested NDC
17856-0166-2
Package NDCs from labels
17856-0166-2, 17856-0166-1, 17856-0166-4, 17856-0166-3, 17856-0166-8, 17856-0166-7, 17856-0166-6, 17856-0166-5
Manufacturer
ATLANTIC BIOLOGICALS CORP | UNIT DOSE SOLUTIONS
Effective date
2023-03-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ACETAMINOPHEN - ATLANTIC BIOLOGICALS CORP | UNIT DOSE SOLUTIONSATLANTIC BIOLOGICALS CORP | UNIT DOSE SOLUTIONS2023-03-13HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDCRelated label
17856-0166-1Acetaminophen Elxir Bubble Gum Flavor
17856-0166-3Acetaminophen Elxir Bubble Gum Flavor
17856-0166-5Acetaminophen Elxir Bubble Gum Flavor
17856-0166-7Acetaminophen Elxir Bubble Gum Flavor

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-0166-1ACETAMINOPHEN72 in 1 BOX, UNIT-DOSEELIXIR722
17856-0166-2ACETAMINOPHEN10.15 mL in 1 CUP, UNIT-DOSEELIXIR10.152
17856-0166-3ACETAMINOPHEN50 in 1 BOX, UNIT-DOSEELIXIR502
17856-0166-4ACETAMINOPHEN20.31 mL in 1 CUP, UNIT-DOSEELIXIR20.312
17856-0166-5ACETAMINOPHEN72 in 1 BOX, UNIT-DOSEELIXIR722
17856-0166-6ACETAMINOPHEN15 mL in 1 CUP, UNIT-DOSEELIXIR152
17856-0166-7ACETAMINOPHEN50 in 1 BOX, UNIT-DOSEELIXIR502
17856-0166-8ACETAMINOPHEN31.2 mL in 1 CUP, UNIT-DOSEELIXIR31.22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-0166ACETAMINOPHEN ELIXIR [ATLANTIC BIOLOGICALS CORP]2Legacy NDC, 8 package rows20230314_57b9b32c-6a5c-49d7-b4df-e0489a98168c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17856-0166-1ML - Milliliter17856-01669225ee42-5e40-417c-8084-dfcad7bff92412023-06-06
17856-0166-3ML - Milliliter17856-0166be1d41bb-feef-4f75-ae3e-15c3a339c1eb12023-06-06
17856-0166-5ML - Milliliter17856-0166067cab20-451e-4e77-a8da-8838f258b66b12023-06-06

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 36 of 181 · 3,619 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EXTRA STRENGTH PAIN RELIEFACETAMINOPHENPreferred Pharmaceuticals Inc.e18294f5-8fd5-4ac6-802c-f6d257e8bee72026-04-15WarningsExact identifier
unii: 362O9ITL9D
AcetaminophenACETAMINOPHENPreferred Pharmaceuticals Inc.b6abfbbb-9826-4cd6-940f-3a314480a5a52026-04-15WarningsExact identifier
unii: 362O9ITL9D
Good Sense Pain ReliefACETAMINOPHENPreferred Pharmaceuticals Inc.36708cac-c076-4514-bfa1-9db6918749002026-04-15WarningsExact identifier
unii: 362O9ITL9D
Sinus and HeadacheACETAMINOPHEN, PHENYLEPHRINE HCLWalgreen Company2115f095-2d75-4e02-a6af-22dd693e08402026-04-14WarningsExact identifier
unii: 362O9ITL9D
daytime severe cold and fluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDECVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED5515148f-3e1d-4b03-89fa-40967d5082922026-04-14WarningsExact identifier
unii: 362O9ITL9D
Good Sense Pain and FeverACETAMINOPHENL. Perrigo Companyf7137fe6-582e-43a4-8302-90ca54cd1de32026-04-14WarningsExact identifier
unii: 362O9ITL9D
Mucus Relief Sinus Severe Congestion and PainACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDc70e6506-6c5b-4d3f-ab18-a690840caabc2026-04-13WarningsExact identifier
unii: 362O9ITL9D
AcetaminophenACETAMINOPHENCardinal Health 107, LLCe13656eb-513e-411e-bdae-35ff1ba7cfc12026-04-13WarningsExact identifier
rxcui: 307675
unii: 362O9ITL9D
Artificial Tears Lubricant Eye DropsGLYCERIN, PROPYLENE GLYCOLCVS Pharmacy28297fee-8185-4869-8f39-5bfbf8bf8bfd2026-04-13WarningsExact identifier
unii: PDC6A3C0OX
blink boostGLYCERINBausch & Lomb Incorporatede765c224-1718-488f-99b2-976eb60c1d632026-04-13WarningsExact identifier
unii: PDC6A3C0OX
OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHENBryant Ranch Prepack3339d3bd-b416-4c5b-8984-0c376544d8a92026-04-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
Severe Sinus CongestionACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCLWalgreen Company8745d9d8-640d-4e3b-96fe-d25032c1e3ce2026-04-13WarningsExact identifier
unii: 362O9ITL9D
Retaine Ultra PFPOLYETHYLENE GLYCOLOCuSOFT LLCa5aaaf06-772d-44d3-8601-f978ddc48ad72026-04-13WarningsExact identifier
unii: B697894SGQ
BUTALBITAL, ACETAMINOPHEN AND CAFFEINEBUTALBITAL, ACETAMINOPHEN AND CAFFEINEAmici Pharma, Inc.fb12459c-82f8-43d2-8c05-a4b6d4a3e9482026-04-13Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
CareOne AcetaminophenACETAMINOPHENAmerican Sales Companyb4f54465-3232-4685-9570-90be008765772026-04-12WarningsExact identifier
unii: 362O9ITL9D
Daytime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HCLBETTER LIVING BRANDS, LLC46adbf94-5b93-ee64-e063-6294a90a11442026-04-11WarningsExact identifier
unii: 362O9ITL9D
Childrens Pain Relief Dye freeACTEMINOPHENBETTER LIVING BRANDS LLC.41f504d1-29c4-f075-e063-6394a90ad64c2026-04-11WarningsExact identifier
unii: 362O9ITL9D
Tramadol/APAPTRAMADOL/APAPDirect_rx4e40f55e-1d8e-ce2f-e063-6294a90a7bec2026-04-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 362O9ITL9D
AcetaminophenACETAMINOPHENMedline Industries, LP9f18d455-55ce-482c-8da8-dcb664038c6c2026-04-10WarningsExact identifier
unii: 362O9ITL9D
Dr. Simi Pain Reliever PMACETAMINOPHEN, DIPHENHYDRAMINE HCLFarmacias De Similares TX LLC4f1e1f1a-44f4-2356-e063-6294a90a8cdd2026-04-10WarningsExact identifier
unii: 362O9ITL9D

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.