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Family Wellness Sensitive Extra Whitening
Family Wellness Sensitive Extra Whitening - 55319-900-01 - (Potassium Nitrate and Sodium Fluoride)
Drug Information of Family Wellness Sensitive Extra Whitening
| Product NDC: | 55319-900 |
| Proprietary Name: | Family Wellness Sensitive Extra Whitening |
| Non Proprietary Name: | Potassium Nitrate and Sodium Fluoride |
| Active Ingredient(s): | 5; 1.5 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 Family Wellness Sensitive Extra Whitening
| Product NDC: | 55319-900 |
| Labeler Name: | Family Wellness |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130411 |
Package Information of Family Wellness Sensitive Extra Whitening
| Package NDC: | 55319-900-01 |
| Package Description: | 113 g in 1 TUBE (55319-900-01) |
NDC Information of Family Wellness Sensitive Extra Whitening
| NDC Code | 55319-900-01 |
| Proprietary Name | Family Wellness Sensitive Extra Whitening |
| Package Description | 113 g in 1 TUBE (55319-900-01) |
| Product NDC | 55319-900 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium Nitrate and Sodium Fluoride |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20130411 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Family Wellness |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 5; 1.5 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
