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Formo Cresol
Formo Cresol - 0699-0001-01 - (Cresol)
Drug Information of Formo Cresol
| Product NDC: | 0699-0001 |
| Proprietary Name: | Formo Cresol |
| Non Proprietary Name: | Cresol |
| Active Ingredient(s): | 485 mg/g & nbsp; Cresol |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Formo Cresol
| Product NDC: | 0699-0001 |
| Labeler Name: | DSHealthcare |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19630219 |
Package Information of Formo Cresol
| Package NDC: | 0699-0001-01 |
| Package Description: | 33.57 g in 1 BOTTLE, GLASS (0699-0001-01) |
NDC Information of Formo Cresol
| NDC Code | 0699-0001-01 |
| Proprietary Name | Formo Cresol |
| Package Description | 33.57 g in 1 BOTTLE, GLASS (0699-0001-01) |
| Product NDC | 0699-0001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cresol |
| Dosage Form Name | LIQUID |
| Route Name | DENTAL |
| Start Marketing Date | 19630219 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | DSHealthcare |
| Substance Name | CRESOL |
| Strength Number | 485 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Standardized Chemical Allergen [EPC] |
