| Product NDC: | 15304-4182 |
| Proprietary Name: | Mastic Dent Whitening |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 2.2 mg/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL; ORAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 15304-4182 |
| Labeler Name: | Chia Gi LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20051122 |
| Package NDC: | 15304-4182-1 |
| Package Description: | 75 mL in 1 TUBE (15304-4182-1) |
| NDC Code | 15304-4182-1 |
| Proprietary Name | Mastic Dent Whitening |
| Package Description | 75 mL in 1 TUBE (15304-4182-1) |
| Product NDC | 15304-4182 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL; ORAL |
| Start Marketing Date | 20051122 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Chia Gi LTD |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |