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Original Antiseptic - 36800-318-12 - (EUCALYPTOL)

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Drug Information of Original Antiseptic

Product NDC: 36800-318
Proprietary Name: Original Antiseptic
Non Proprietary Name: EUCALYPTOL
Active Ingredient(s): .092; .042; .06; .064    kg/100L; kg/100L; kg/100L; kg/100L & nbsp;   EUCALYPTOL
Administration Route(s): ORAL
Dosage Form(s): MOUTHWASH
Coding System: National Drug Codes(NDC)

Labeler Information of Original Antiseptic

Product NDC: 36800-318
Labeler Name: Topco Associates, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part356
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19900715

Package Information of Original Antiseptic

Package NDC: 36800-318-12
Package Description: 1.5 L in 1 BOTTLE, PLASTIC (36800-318-12)

NDC Information of Original Antiseptic

NDC Code 36800-318-12
Proprietary Name Original Antiseptic
Package Description 1.5 L in 1 BOTTLE, PLASTIC (36800-318-12)
Product NDC 36800-318
Product Type Name HUMAN OTC DRUG
Non Proprietary Name EUCALYPTOL
Dosage Form Name MOUTHWASH
Route Name ORAL
Start Marketing Date 19900715
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Topco Associates, LLC
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 Original Antiseptic


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