Up and Up Childrens Ibuprofen
Target Corporation Children’s Ibuprofen Drug Facts
Approved
Approval ID
eead7d57-dfd3-4007-a620-74afebc3d365
Product Type
HUMAN OTC DRUG LABEL
Effective Date
May 4, 2025
Manufacturers
FDA
Target Corporation
DUNS: 006961700
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ibuprofen
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code11673-593
Application NumberANDA076359
Product Classification
M
Marketing Category
C73584
G
Generic Name
ibuprofen
Product Specifications
Route of AdministrationORAL
Effective DateMay 4, 2025
FDA Product Classification
INGREDIENTS (14)
IBUPROFENActive
Quantity: 100 mg in 1 1
Code: WK2XYI10QM
Classification: ACTIB
ACESULFAME POTASSIUMInactive
Code: 23OV73Q5G9
Classification: IACT
AMMONIUM GLYCYRRHIZATEInactive
Code: 3VRD35U26C
Classification: IACT
ASPARTAMEInactive
Code: Z0H242BBR1
Classification: IACT
CARNAUBA WAXInactive
Code: R12CBM0EIZ
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
FD&C YELLOW NO. 6 ALUMINUM LAKEInactive
Code: GYP6Z2JR6Q
Classification: IACT
HYPROMELLOSE, UNSPECIFIEDInactive
Code: 3NXW29V3WO
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
SODIUM LAURYL SULFATEInactive
Code: 368GB5141J
Classification: IACT
SOYBEAN OILInactive
Code: 241ATL177A
Classification: IACT
SUCCINIC ACIDInactive
Code: AB6MNQ6J6L
Classification: IACT