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Anticavity Fluoride Rinse
Anticavity Fluoride Rinse - 75981-213-44 - (SODIUM FLUORIDE)
Drug Information of Anticavity Fluoride Rinse
| Product NDC: | 75981-213 |
| Proprietary Name: | Anticavity Fluoride Rinse |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .05 kg/100L & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anticavity Fluoride Rinse
| Product NDC: | 75981-213 |
| Labeler Name: | Geiss, Destin + Dunn, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20070817 |
Package Information of Anticavity Fluoride Rinse
| Package NDC: | 75981-213-44 |
| Package Description: | .532 L in 1 BOTTLE, PLASTIC (75981-213-44) |
NDC Information of Anticavity Fluoride Rinse
| NDC Code | 75981-213-44 |
| Proprietary Name | Anticavity Fluoride Rinse |
| Package Description | .532 L in 1 BOTTLE, PLASTIC (75981-213-44) |
| Product NDC | 75981-213 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | MOUTHWASH |
| Route Name | ORAL |
| Start Marketing Date | 20070817 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Geiss, Destin + Dunn, Inc |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .05 |
| Strength Unit | kg/100L |
| Pharmaceutical Classes |
