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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code82725-3103
Application NumberANDA077829
Product Classification
M
Marketing Category
C73584
G
Generic Name
CETIRIZINE HYDROCHLORIDE
Product Specifications
Route of AdministrationORAL
Effective DateApril 7, 2025
FDA Product Classification
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