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Opalescence PF
Opalescence PF - 51206-303-07 - (Sodium Fluoride and Potassium Nitrate)
Drug Information of Opalescence PF
| Product NDC: | 51206-303 |
| Proprietary Name: | Opalescence PF |
| Non Proprietary Name: | Sodium Fluoride and Potassium Nitrate |
| Active Ingredient(s): | 1.4175; .070875 g/28.35g; g/28.35g & nbsp; Sodium Fluoride and Potassium Nitrate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Opalescence PF
| Product NDC: | 51206-303 |
| Labeler Name: | Ultradent Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101115 |
Package Information of Opalescence PF
| Package NDC: | 51206-303-07 |
| Package Description: | 1 TUBE in 1 BOX (51206-303-07) > 28.35 g in 1 TUBE |
NDC Information of Opalescence PF
| NDC Code | 51206-303-07 |
| Proprietary Name | Opalescence PF |
| Package Description | 1 TUBE in 1 BOX (51206-303-07) > 28.35 g in 1 TUBE |
| Product NDC | 51206-303 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride and Potassium Nitrate |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20101115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultradent Products, Inc. |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 1.4175; .070875 |
| Strength Unit | g/28.35g; g/28.35g |
| Pharmaceutical Classes |
