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Budpak Medicated Anti Itch - 27293-027-01 - (Camphor and Menthol)

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Drug Information of Budpak Medicated Anti Itch

Product NDC: 27293-027
Proprietary Name: Budpak Medicated Anti Itch
Non Proprietary Name: Camphor and Menthol
Active Ingredient(s): .01; .01    g/g; g/g & nbsp;   Camphor and Menthol
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Budpak Medicated Anti Itch

Product NDC: 27293-027
Labeler Name: Budpak Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121217

Package Information of Budpak Medicated Anti Itch

Package NDC: 27293-027-01
Package Description: 1 TUBE in 1 BOX (27293-027-01) > 28 g in 1 TUBE (27293-027-28)

NDC Information of Budpak Medicated Anti Itch

NDC Code 27293-027-01
Proprietary Name Budpak Medicated Anti Itch
Package Description 1 TUBE in 1 BOX (27293-027-01) > 28 g in 1 TUBE (27293-027-28)
Product NDC 27293-027
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Camphor and Menthol
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121217
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Budpak Inc.
Substance Name CAMPHOR (SYNTHETIC); MENTHOL
Strength Number .01; .01
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of Budpak Medicated Anti Itch


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