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Up and Up Sensitive Toothpaste Whitening
Up and Up Sensitive Toothpaste Whitening - 67659-079-02 - (Potassium Nitrate and Sodium Fluoride)
Drug Information of Up and Up Sensitive Toothpaste Whitening
| Product NDC: | 67659-079 |
| Proprietary Name: | Up and Up Sensitive Toothpaste Whitening |
| Non Proprietary Name: | Potassium Nitrate and Sodium Fluoride |
| Active Ingredient(s): | 5; 2.43 mg/g; mg/g & nbsp; Potassium Nitrate and Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Up and Up Sensitive Toothpaste Whitening
| Product NDC: | 67659-079 |
| Labeler Name: | Team Technologies, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100825 |
Package Information of Up and Up Sensitive Toothpaste Whitening
| Package NDC: | 67659-079-02 |
| Package Description: | 1 TUBE in 1 CARTON (67659-079-02) > 113 g in 1 TUBE (67659-079-01) |
NDC Information of Up and Up Sensitive Toothpaste Whitening
| NDC Code | 67659-079-02 |
| Proprietary Name | Up and Up Sensitive Toothpaste Whitening |
| Package Description | 1 TUBE in 1 CARTON (67659-079-02) > 113 g in 1 TUBE (67659-079-01) |
| Product NDC | 67659-079 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium Nitrate and Sodium Fluoride |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20100825 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Team Technologies, Inc |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 5; 2.43 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
