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Antiseptic Mouth Rinse - 49738-210-12 - (EUCALYPTOL, MENTHOL, METYL SALICYLATE, THYMOL)

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Drug Information of Antiseptic Mouth Rinse

Product NDC: 49738-210
Proprietary Name: Antiseptic Mouth Rinse
Non Proprietary Name: EUCALYPTOL, MENTHOL, METYL SALICYLATE, THYMOL
Active Ingredient(s): .092; .042; .06; .064    kg/100L; kg/100L; kg/100L; kg/100L & nbsp;   EUCALYPTOL, MENTHOL, METYL SALICYLATE, THYMOL
Administration Route(s): ORAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Antiseptic Mouth Rinse

Product NDC: 49738-210
Labeler Name: KMart Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19960821

Package Information of Antiseptic Mouth Rinse

Package NDC: 49738-210-12
Package Description: 1.5 L in 1 BOTTLE, PLASTIC (49738-210-12)

NDC Information of Antiseptic Mouth Rinse

NDC Code 49738-210-12
Proprietary Name Antiseptic Mouth Rinse
Package Description 1.5 L in 1 BOTTLE, PLASTIC (49738-210-12)
Product NDC 49738-210
Product Type Name HUMAN OTC DRUG
Non Proprietary Name EUCALYPTOL, MENTHOL, METYL SALICYLATE, THYMOL
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 19960821
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name KMart Corporation
Substance Name EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Strength Number .092; .042; .06; .064
Strength Unit kg/100L; kg/100L; kg/100L; kg/100L
Pharmaceutical Classes

Complete Information of Antiseptic Mouth Rinse


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