| Product NDC: | 53045-300 |
| Proprietary Name: | Frenna AC |
| Non Proprietary Name: | Aluminum Chloride |
| Active Ingredient(s): | 8.75 g/35g & nbsp; Aluminum Chloride |
| Administration Route(s): | DENTAL; ORAL; TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 53045-300 |
| Labeler Name: | Dharma Research, inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130101 |
| Package NDC: | 53045-300-30 |
| Package Description: | 35 g in 1 BOTTLE, PLASTIC (53045-300-30) |
| NDC Code | 53045-300-30 |
| Proprietary Name | Frenna AC |
| Package Description | 35 g in 1 BOTTLE, PLASTIC (53045-300-30) |
| Product NDC | 53045-300 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aluminum Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | DENTAL; ORAL; TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Dharma Research, inc. |
| Substance Name | ALUMINUM CHLORIDE |
| Strength Number | 8.75 |
| Strength Unit | g/35g |
| Pharmaceutical Classes |