Vexasyn
Vexasyn GelPrescription Only | Rx Only
Approved
Approval ID
741d022f-954f-4686-b60e-08337235e9a7
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 31, 2018
Manufacturers
FDA
Sterling-Knight Pharmaceuticals, LLC
DUNS: 079556942
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Vexasyn
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code69336-831
Application NumberK020540
Product Classification
M
Marketing Category
C80442
Product Specifications
Effective DateJuly 30, 2018
FDA Product Classification
INGREDIENTS (9)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM ALGINATEInactive
Code: C269C4G2ZQ
Classification: IACT
GLYCERINInactive
Code: PDC6A3C0OX
Classification: IACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)Inactive
Code: R33S7TK2EP
Classification: IACT
LIDOCAINE HYDROCHLORIDEInactive
Code: V13007Z41A
Classification: IACT
BENZETHONIUM CHLORIDEInactive
Code: PH41D05744
Classification: IACT
TROLAMINEInactive
Code: 9O3K93S3TK
Classification: IACT
ALOE VERA LEAFInactive
Code: ZY81Z83H0X
Classification: IACT
BOVINE TYPE I COLLAGENInactive
Code: FHJ3ATL51C
Classification: IACT