| 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 |