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Menthol and Zinc Oxide - 67777-234-01 - (Menthol and Zinc Oxide)

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Drug Information of Menthol and Zinc Oxide

Product NDC: 67777-234
Proprietary Name: Menthol and Zinc Oxide
Non Proprietary Name: Menthol and Zinc Oxide
Active Ingredient(s): .44; 21    g/100g; g/100g & nbsp;   Menthol and Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Menthol and Zinc Oxide

Product NDC: 67777-234
Labeler Name: Dynarex Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part347
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100511

Package Information of Menthol and Zinc Oxide

Package NDC: 67777-234-01
Package Description: 2 BOX in 1 CASE (67777-234-01) > 144 POUCH in 1 BOX > 3.5 g in 1 POUCH

NDC Information of Menthol and Zinc Oxide

NDC Code 67777-234-01
Proprietary Name Menthol and Zinc Oxide
Package Description 2 BOX in 1 CASE (67777-234-01) > 144 POUCH in 1 BOX > 3.5 g in 1 POUCH
Product NDC 67777-234
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol and Zinc Oxide
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20100511
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dynarex Corporation
Substance Name MENTHOL; ZINC OXIDE
Strength Number .44; 21
Strength Unit g/100g; g/100g
Pharmaceutical Classes

Complete Information of Menthol and Zinc Oxide


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