Product NDC: | 67659-041 |
Proprietary Name: | Laura Lynn Anticavity |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | 2.43 mg/g & nbsp; Sodium Fluoride |
Administration Route(s): | DENTAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67659-041 |
Labeler Name: | Team Technologies, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part355 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20060829 |
Package NDC: | 67659-041-05 |
Package Description: | 181.4 g in 1 TUBE (67659-041-05) |
NDC Code | 67659-041-05 |
Proprietary Name | Laura Lynn Anticavity |
Package Description | 181.4 g in 1 TUBE (67659-041-05) |
Product NDC | 67659-041 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | PASTE |
Route Name | DENTAL |
Start Marketing Date | 20060829 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Team Technologies, Inc |
Substance Name | SODIUM FLUORIDE |
Strength Number | 2.43 |
Strength Unit | mg/g |
Pharmaceutical Classes |