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Hemoban
Hemoban - 0699-1082-08 - (Aluminum Chloride)
Drug Information of Hemoban
| Product NDC: | 0699-1082 |
| Proprietary Name: | Hemoban |
| Non Proprietary Name: | Aluminum Chloride |
| Active Ingredient(s): | 250 mg/g & nbsp; Aluminum Chloride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hemoban
| Product NDC: | 0699-1082 |
| Labeler Name: | DSHealthcare |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19630219 |
Package Information of Hemoban
| Package NDC: | 0699-1082-08 |
| Package Description: | 4490.9 g in 1 BOTTLE, GLASS (0699-1082-08) |
NDC Information of Hemoban
| NDC Code | 0699-1082-08 |
| Proprietary Name | Hemoban |
| Package Description | 4490.9 g in 1 BOTTLE, GLASS (0699-1082-08) |
| Product NDC | 0699-1082 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aluminum Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | DENTAL |
| Start Marketing Date | 19630219 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | DSHealthcare |
| Substance Name | ALUMINUM CHLORIDE |
| Strength Number | 250 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
