Cabinet All Day Allergy Relief
Cabinet All Day Allergy Relief Cetirizine Hydrochloride
Approved
Approval ID
889316bc-5f98-426a-9750-2fdb0c427408
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Apr 7, 2025
Manufacturers
FDA
Cabinet Health P.B.C.
DUNS: 117102391
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
CETIRIZINE HYDROCHLORIDE
PRODUCT DETAILS
NDC Product Code82725-3103
Application NumberANDA077829
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 7, 2025
Generic NameCETIRIZINE HYDROCHLORIDE
INGREDIENTS (8)
HYPROMELLOSE, UNSPECIFIEDInactive
Code: 3NXW29V3WO
Classification: IACT
LACTOSEInactive
Code: J2B2A4N98G
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
POLYETHYLENE GLYCOL, UNSPECIFIEDInactive
Code: 3WJQ0SDW1A
Classification: IACT
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
CETIRIZINE HYDROCHLORIDEActive
Quantity: 10 mg in 1 1
Code: 64O047KTOA
Classification: ACTIM