| Product NDC: | 58701-001 |
| Proprietary Name: | First Class Kit |
| Non Proprietary Name: | Sodium Monofluorophosphate |
| Active Ingredient(s): | 7.6 mg/g & nbsp; Sodium Monofluorophosphate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58701-001 |
| Labeler Name: | American Airlines, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130510 |
| Package NDC: | 58701-001-10 |
| Package Description: | 1 TUBE in 1 PACKAGE (58701-001-10) > 10 g in 1 TUBE |
| NDC Code | 58701-001-10 |
| Proprietary Name | First Class Kit |
| Package Description | 1 TUBE in 1 PACKAGE (58701-001-10) > 10 g in 1 TUBE |
| Product NDC | 58701-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Monofluorophosphate |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20130510 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | American Airlines, Inc. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 7.6 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |