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Pure Snow whitening
Pure Snow whitening - 52893-001-01 - (Sodium Fluoride)
Drug Information of Pure Snow whitening
| Product NDC: | 52893-001 |
| Proprietary Name: | Pure Snow whitening |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .07 g/28.35g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pure Snow whitening
| Product NDC: | 52893-001 |
| Labeler Name: | Itena Clinical |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121130 |
Package Information of Pure Snow whitening
| Package NDC: | 52893-001-01 |
| Package Description: | 28.35 g in 1 TUBE (52893-001-01) |
NDC Information of Pure Snow whitening
| NDC Code | 52893-001-01 |
| Proprietary Name | Pure Snow whitening |
| Package Description | 28.35 g in 1 TUBE (52893-001-01) |
| Product NDC | 52893-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20121130 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Itena Clinical |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .07 |
| Strength Unit | g/28.35g |
| Pharmaceutical Classes |
