| Product NDC: | 48871-180 |
| Proprietary Name: | Live Better |
| Non Proprietary Name: | Fluoride |
| Active Ingredient(s): | 5; .24 g/100g; g/100g & nbsp; Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 48871-180 |
| Labeler Name: | Health Tech Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110120 |
| Package NDC: | 48871-180-09 |
| Package Description: | 1 TUBE in 1 CARTON (48871-180-09) > 113 g in 1 TUBE (48871-180-02) |
| NDC Code | 48871-180-09 |
| Proprietary Name | Live Better |
| Package Description | 1 TUBE in 1 CARTON (48871-180-09) > 113 g in 1 TUBE (48871-180-02) |
| Product NDC | 48871-180 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110120 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Health Tech Inc |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 5; .24 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |