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Antiseptic Mouthrinse - 49035-072-69 - (Eucalyptol, Menthol, Methyl salicylate, Thymol)

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Drug Information of Antiseptic Mouthrinse

Product NDC: 49035-072
Proprietary Name: Antiseptic Mouthrinse
Non Proprietary Name: Eucalyptol, Menthol, Methyl salicylate, Thymol
Active Ingredient(s): .092; .042; .06; .064    kg/100L; kg/100L; kg/100L; kg/100L & nbsp;   Eucalyptol, Menthol, Methyl salicylate, Thymol
Administration Route(s): ORAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Antiseptic Mouthrinse

Product NDC: 49035-072
Labeler Name: Wal-Mart Stores, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19891111

Package Information of Antiseptic Mouthrinse

Package NDC: 49035-072-69
Package Description: .25 L in 1 BOTTLE, PLASTIC (49035-072-69)

NDC Information of Antiseptic Mouthrinse

NDC Code 49035-072-69
Proprietary Name Antiseptic Mouthrinse
Package Description .25 L in 1 BOTTLE, PLASTIC (49035-072-69)
Product NDC 49035-072
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Eucalyptol, Menthol, Methyl salicylate, Thymol
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 19891111
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Wal-Mart Stores, Inc.
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 Mouthrinse


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