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Tartar control plus - 0869-0434-12 - (Eucalyptol, menthol, methyl salicylate, thymol)

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Drug Information of Tartar control plus

Product NDC: 0869-0434
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: 0869-0434
Labeler Name: Vi-Jon
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130610

Package Information of Tartar control plus

Package NDC: 0869-0434-12
Package Description: 1499 mL in 1 BOTTLE, PLASTIC (0869-0434-12)

NDC Information of Tartar control plus

NDC Code 0869-0434-12
Proprietary Name Tartar control plus
Package Description 1499 mL in 1 BOTTLE, PLASTIC (0869-0434-12)
Product NDC 0869-0434
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Eucalyptol, menthol, methyl salicylate, thymol
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 20130610
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Vi-Jon
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

Complete Information of Tartar control plus


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