MedPath
FDA Product

lumicain

Product approved by U.S. Food and Drug Administration (US)

Basic Information

lumicain

10733-412

Regulatory Information

10733-412

December 23, 2020

lumicain Topical Hemostatic Solution

HUMAN PRESCRIPTION DRUG LABEL

4

Company Information

002290302

Active Ingredients

WATER

Code: 059QF0KO0R

Class Code: IACT

ALUMINUM CHLORIDE

Quantity: 250 mg in 1 g

Code: 3CYT62D3GA

Class Code: ACTIB

Active Moieties

ALUMINUM CATION

Code: 3XHB1D032B

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