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Tartar Control Plus
Tartar Control Plus - 37808-003-86 - (eucalyptol, menthol, methyl salicylate, thymol)
Drug Information of Tartar Control Plus
| Product NDC: | 37808-003 |
| 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) |
Labeler Information of Tartar Control Plus
| Product NDC: | 37808-003 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130601 |
Package Information of Tartar Control Plus
| Package NDC: | 37808-003-86 |
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (37808-003-86) |
NDC Information of Tartar Control Plus
| NDC Code | 37808-003-86 |
| Proprietary Name | Tartar Control Plus |
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (37808-003-86) |
| Product NDC | 37808-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | eucalyptol, menthol, methyl salicylate, thymol |
| Dosage Form Name | MOUTHWASH |
| Route Name | ORAL |
| Start Marketing Date | 20130601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| 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 |
