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Formo Cresol

Formocresol/Buckley's Formocresol

Approved
Approval ID

6989bddc-910e-47e6-aa8f-619a330e81b8

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Feb 4, 2010

Manufacturers
FDA

DSHealthcare

DUNS: 056296981

Products 2

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Cresol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0699-0412
Product Classification
G
Generic Name
Cresol
Product Specifications
Route of AdministrationDENTAL
Effective DateFebruary 4, 2010
FDA Product Classification

INGREDIENTS (2)

GlycerinInactive
Code: PDC6A3C0OX
Classification: IACT
CresolActive
Quantity: 485 mg in 1 g
Code: GF3CGH8D7Z
Classification: ACTIM

Cresol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0699-0001
Product Classification
G
Generic Name
Cresol
Product Specifications
Route of AdministrationDENTAL
Effective DateFebruary 4, 2010
FDA Product Classification

INGREDIENTS (2)

CresolActive
Quantity: 485 mg in 1 g
Code: GF3CGH8D7Z
Classification: ACTIM
GlycerinInactive
Code: PDC6A3C0OX
Classification: IACT

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Formo Cresol - FDA Drug Approval Details