MedPath

Hemostat

Approved
Approval ID

fcc68d20-efc3-4c1b-9517-39f603c16084

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 19, 2022

Manufacturers
FDA

Pearson Dental Supplies INC.

DUNS: 082874108

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 Code43305-0000
Product Classification
G
Generic Name
Aluminum Chloride
Product Specifications
Route of AdministrationDENTAL
Effective DateJanuary 19, 2022
FDA Product Classification

INGREDIENTS (5)

WATERInactive
Code: 059QF0KO0R
Classification: IACT
DMDM HYDANTOINInactive
Code: BYR0546TOW
Classification: IACT
PROPYLENE GLYCOLInactive
Code: 6DC9Q167V3
Classification: IACT
POTASSIUM CHLORIDEInactive
Code: 660YQ98I10
Classification: IACT
ALUMINUM CHLORIDEActive
Quantity: 7500 mg in 30 mL
Code: 3CYT62D3GA
Classification: ACTIB

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Hemostat - FDA Drug Approval Details