| Product NDC: | 59779-855 |
| Proprietary Name: | Tartar control plus |
| Non Proprietary Name: | Eucalyptol, menthol, methyl salicylate, thymol |
| Active Ingredient(s): | .92; .42; .6; .64 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Eucalyptol, menthol, methyl salicylate, thymol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-855 |
| Labeler Name: | CVS Pharmacy, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130105 |
| Package NDC: | 59779-855-86 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (59779-855-86) |
| NDC Code | 59779-855-86 |
| Proprietary Name | Tartar control plus |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (59779-855-86) |
| Product NDC | 59779-855 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Eucalyptol, menthol, methyl salicylate, thymol |
| Dosage Form Name | MOUTHWASH |
| Route Name | ORAL |
| Start Marketing Date | 20130105 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CVS Pharmacy, Inc |
| Substance Name | EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL |
| Strength Number | .92; .42; .6; .64 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |