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Crest Sensitivity
Crest Sensitivity - 37000-519-02 - (Potassium nitrate and Sodium Fluoride)
Drug Information of Crest Sensitivity
| Product NDC: | 37000-519 |
| Proprietary Name: | Crest Sensitivity |
| Non Proprietary Name: | Potassium nitrate and Sodium Fluoride |
| Active Ingredient(s): | .05; 243 g/g; g/g & nbsp; Potassium nitrate and Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Crest Sensitivity
| Product NDC: | 37000-519 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100830 |
Package Information of Crest Sensitivity
| Package NDC: | 37000-519-02 |
| Package Description: | 1 TUBE in 1 CARTON (37000-519-02) > 24 g in 1 TUBE (37000-519-01) |
NDC Information of Crest Sensitivity
| NDC Code | 37000-519-02 |
| Proprietary Name | Crest Sensitivity |
| Package Description | 1 TUBE in 1 CARTON (37000-519-02) > 24 g in 1 TUBE (37000-519-01) |
| Product NDC | 37000-519 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium nitrate and Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20100830 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | .05; 243 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |
