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Hemostat

Approved
Approval ID

ddb206ac-28ed-48ac-8d78-88e95cf03918

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 1, 2019

Manufacturers
FDA

Cargus International, Inc.

DUNS: 096191093

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 Code61509-100
Product Classification
G
Generic Name
Aluminum Chloride
Product Specifications
Route of AdministrationDENTAL
Effective DateFebruary 1, 2019
FDA Product Classification

INGREDIENTS (5)

DMDM HYDANTOINInactive
Code: BYR0546TOW
Classification: IACT
Propylene GlycolInactive
Code: 6DC9Q167V3
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT
Aluminum ChlorideActive
Quantity: 7500 mg in 30 mL
Code: 3CYT62D3GA
Classification: ACTIB
Potassium ChlorideInactive
Code: 660YQ98I10
Classification: IACT

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Hemostat - FDA Drug Approval Details