| Product NDC: | 48878-0231 |
| Proprietary Name: | Avagard D |
| Non Proprietary Name: | alcohol |
| Active Ingredient(s): | 530.7 mg/mL & nbsp; alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 48878-0231 |
| Labeler Name: | 3M ESPE Dental Products |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19991001 |
| Package NDC: | 48878-0231-7 |
| Package Description: | 12 BOTTLE in 1 CASE (48878-0231-7) > 500 mL in 1 BOTTLE |
| NDC Code | 48878-0231-7 |
| Proprietary Name | Avagard D |
| Package Description | 12 BOTTLE in 1 CASE (48878-0231-7) > 500 mL in 1 BOTTLE |
| Product NDC | 48878-0231 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | alcohol |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19991001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | 3M ESPE Dental Products |
| Substance Name | ALCOHOL |
| Strength Number | 530.7 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |