| Product NDC: | 41167-0968 | 
| Proprietary Name: | ACT Total Care Dry Mouth Anticavity Mouth | 
| Non Proprietary Name: | Sodium Fluoride | 
| Active Ingredient(s): | .2 mg/mL & nbsp; Sodium Fluoride | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | RINSE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 41167-0968 | 
| Labeler Name: | Chattem, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part355 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20110201 | 
| Package NDC: | 41167-0968-3 | 
| Package Description: | 1000 mL in 1 BOTTLE (41167-0968-3) | 
| NDC Code | 41167-0968-3 | 
| Proprietary Name | ACT Total Care Dry Mouth Anticavity Mouth | 
| Package Description | 1000 mL in 1 BOTTLE (41167-0968-3) | 
| Product NDC | 41167-0968 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Sodium Fluoride | 
| Dosage Form Name | RINSE | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110201 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Chattem, Inc. | 
| Substance Name | SODIUM FLUORIDE | 
| Strength Number | .2 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes |