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Crest Cavity Protection
Crest Cavity Protection - 37000-005-08 - (Sodium Fluoride)
Drug Information of Crest Cavity Protection
| Product NDC: | 37000-005 |
| Proprietary Name: | Crest Cavity Protection |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 2.43 mg/g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Crest Cavity Protection
| Product NDC: | 37000-005 |
| Labeler Name: | Procter & Gamble Manfuacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19840802 |
Package Information of Crest Cavity Protection
| Package NDC: | 37000-005-08 |
| Package Description: | 1 TUBE in 1 CARTON (37000-005-08) > 24 g in 1 TUBE (37000-005-10) |
NDC Information of Crest Cavity Protection
| NDC Code | 37000-005-08 |
| Proprietary Name | Crest Cavity Protection |
| Package Description | 1 TUBE in 1 CARTON (37000-005-08) > 24 g in 1 TUBE (37000-005-10) |
| Product NDC | 37000-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 19840802 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manfuacturing Company |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.43 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
