| Product NDC: | 0273-7002 |
| Proprietary Name: | Perfect Choice |
| Non Proprietary Name: | Sodium Fluoride and Hydrofluoric Acid |
| Active Ingredient(s): | 4.4; 7.9 mg/g; mg/g & nbsp; Sodium Fluoride and Hydrofluoric Acid |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0273-7002 |
| Labeler Name: | Young Dental Manufacturing Co 1, LLC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20060831 |
| Package NDC: | 0273-7002-16 |
| Package Description: | 497 g in 1 BOTTLE (0273-7002-16) |
| NDC Code | 0273-7002-16 |
| Proprietary Name | Perfect Choice |
| Package Description | 497 g in 1 BOTTLE (0273-7002-16) |
| Product NDC | 0273-7002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride and Hydrofluoric Acid |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20060831 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Young Dental Manufacturing Co 1, LLC. |
| Substance Name | HYDROFLUORIC ACID; SODIUM FLUORIDE |
| Strength Number | 4.4; 7.9 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |