lumicain
lumicain Topical Hemostatic Solution
Approved
Approval ID
9fdcce3e-e4d4-41ae-8609-37987c12414e
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 23, 2020
Manufacturers
FDA
Medical Products Laboratories, Inc.
DUNS: 002290302
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Aluminium Chloride Hexahydrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10733-412
Product Classification
G
Generic Name
Aluminium Chloride Hexahydrate
Product Specifications
Route of AdministrationTOPICAL
Effective DateDecember 23, 2020
FDA Product Classification
INGREDIENTS (2)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ALUMINUM CHLORIDEActive
Quantity: 250 mg in 1 g
Code: 3CYT62D3GA
Classification: ACTIB