Product NDC: | 27293-030 |
Proprietary Name: | Budpack |
Non Proprietary Name: | Menthol |
Active Ingredient(s): | 2.5 g/100g & nbsp; Menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 27293-030 |
Labeler Name: | Budpack Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120630 |
Package NDC: | 27293-030-35 |
Package Description: | 35 g in 1 TUBE (27293-030-35) |
NDC Code | 27293-030-35 |
Proprietary Name | Budpack |
Package Description | 35 g in 1 TUBE (27293-030-35) |
Product NDC | 27293-030 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Menthol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20120630 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Budpack Inc. |
Substance Name | MENTHOL |
Strength Number | 2.5 |
Strength Unit | g/100g |
Pharmaceutical Classes |