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Rite Aid Sensitive Toothpaste Extra Whitening
Rite Aid Sensitive Toothpaste Extra Whitening - 11822-0821-1 - (Potassium Nitrate and Sodium Fluoride)
Drug Information of Rite Aid Sensitive Toothpaste Extra Whitening
| Product NDC: | 11822-0821 |
| Proprietary Name: | Rite Aid Sensitive Toothpaste Extra 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 Rite Aid Sensitive Toothpaste Extra Whitening
| Product NDC: | 11822-0821 |
| Labeler Name: | Rite Aid |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100830 |
Package Information of Rite Aid Sensitive Toothpaste Extra Whitening
| Package NDC: | 11822-0821-1 |
| Package Description: | 113 g in 1 TUBE (11822-0821-1) |
NDC Information of Rite Aid Sensitive Toothpaste Extra Whitening
| NDC Code | 11822-0821-1 |
| Proprietary Name | Rite Aid Sensitive Toothpaste Extra Whitening |
| Package Description | 113 g in 1 TUBE (11822-0821-1) |
| Product NDC | 11822-0821 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Potassium Nitrate and Sodium Fluoride |
| Dosage Form Name | PASTE |
| Route Name | DENTAL |
| Start Marketing Date | 20100830 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rite Aid |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Strength Number | 5; 2.43 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
