Hemox A
Approved
Approval ID
cf98eb6f-c16e-4541-9d3e-bfaa3a4a5ff2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 20, 2022
Manufacturers
FDA
Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc.
DUNS: 014769301
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Aluminum Chloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68400-203
Product Classification
G
Generic Name
Aluminum Chloride
Product Specifications
Route of AdministrationDENTAL
Effective DateJanuary 20, 2022
FDA Product Classification
INGREDIENTS (5)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
POTASSIUM CHLORIDEInactive
Code: 660YQ98I10
Classification: IACT
DMDM HYDANTOINInactive
Code: BYR0546TOW
Classification: IACT
ALUMINUM CHLORIDEActive
Quantity: 7500 mg in 30 mL
Code: 3CYT62D3GA
Classification: ACTIB