Home > National Drug Code (NDC) > Budpak Feminine Anti-Itch

Budpak Feminine Anti-Itch - 27293-022-01 - (Benzocaine and Resorcinol)

Alphabetical Index


Drug Information of Budpak Feminine Anti-Itch

Product NDC: 27293-022
Proprietary Name: Budpak Feminine Anti-Itch
Non Proprietary Name: Benzocaine and Resorcinol
Active Ingredient(s): .05; .02    g/g; g/g & nbsp;   Benzocaine and Resorcinol
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Budpak Feminine Anti-Itch

Product NDC: 27293-022
Labeler Name: Budpak Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130610

Package Information of Budpak Feminine Anti-Itch

Package NDC: 27293-022-01
Package Description: 1 TUBE in 1 BOX (27293-022-01) > 21.2 g in 1 TUBE (27293-022-21)

NDC Information of Budpak Feminine Anti-Itch

NDC Code 27293-022-01
Proprietary Name Budpak Feminine Anti-Itch
Package Description 1 TUBE in 1 BOX (27293-022-01) > 21.2 g in 1 TUBE (27293-022-21)
Product NDC 27293-022
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzocaine and Resorcinol
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130610
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Budpak Inc.
Substance Name BENZOCAINE; RESORCINOL
Strength Number .05; .02
Strength Unit g/g; g/g
Pharmaceutical Classes

Complete Information of Budpak Feminine Anti-Itch


General Information