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Alcohol-Free Anticavity
Alcohol-Free Anticavity - 59779-482-86 - (Sodium fluoride)
Drug Information of Alcohol-Free Anticavity
| Product NDC: | 59779-482 |
| Proprietary Name: | Alcohol-Free Anticavity |
| Non Proprietary Name: | Sodium fluoride |
| Active Ingredient(s): | .1 mg/mL & nbsp; Sodium fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alcohol-Free Anticavity
| Product NDC: | 59779-482 |
| Labeler Name: | CVS Pharmacy, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120203 |
Package Information of Alcohol-Free Anticavity
| Package NDC: | 59779-482-86 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (59779-482-86) |
NDC Information of Alcohol-Free Anticavity
| NDC Code | 59779-482-86 |
| Proprietary Name | Alcohol-Free Anticavity |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (59779-482-86) |
| Product NDC | 59779-482 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium fluoride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120203 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS Pharmacy, Inc |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
