| Product NDC: | 41167-0940 | 
| Proprietary Name: | ACT Anticavity Fluoride Cinnamon | 
| Non Proprietary Name: | Sodium fluoride | 
| Active Ingredient(s): | .5 mg/mL & nbsp; Sodium fluoride | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | RINSE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 41167-0940 | 
| Labeler Name: | Chattem, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part355 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 19940401 | 
| Package NDC: | 41167-0940-8 | 
| Package Description: | 532 mL in 1 BOTTLE, DISPENSING (41167-0940-8) | 
| NDC Code | 41167-0940-8 | 
| Proprietary Name | ACT Anticavity Fluoride Cinnamon | 
| Package Description | 532 mL in 1 BOTTLE, DISPENSING (41167-0940-8) | 
| Product NDC | 41167-0940 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Sodium fluoride | 
| Dosage Form Name | RINSE | 
| Route Name | TOPICAL | 
| Start Marketing Date | 19940401 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Chattem, Inc. | 
| Substance Name | SODIUM FLUORIDE | 
| Strength Number | .5 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes |