Product NDC: | 14060-006 |
Proprietary Name: | Sheer FluorX PEDO |
Non Proprietary Name: | sodium fluoride |
Active Ingredient(s): | 20 mg/1 & nbsp; sodium fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | FILM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 14060-006 |
Labeler Name: | CAO Group, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110415 |
Package NDC: | 14060-006-03 |
Package Description: | 4 TRAY in 1 PACKAGE (14060-006-03) > 2 FILM in 1 TRAY |
NDC Code | 14060-006-03 |
Proprietary Name | Sheer FluorX PEDO |
Package Description | 4 TRAY in 1 PACKAGE (14060-006-03) > 2 FILM in 1 TRAY |
Product NDC | 14060-006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | sodium fluoride |
Dosage Form Name | FILM |
Route Name | DENTAL |
Start Marketing Date | 20110415 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | CAO Group, Inc. |
Substance Name | SODIUM FLUORIDE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes |