Product NDC: | 0273-7007 |
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: | 0273-7007 |
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: | 0273-7007-16 |
Package Description: | 497 g in 1 BOTTLE (0273-7007-16) |
NDC Code | 0273-7007-16 |
Proprietary Name | Perfect Choice |
Package Description | 497 g in 1 BOTTLE (0273-7007-16) |
Product NDC | 0273-7007 |
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 |