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