| Product NDC: | 63940-100 |
| Proprietary Name: | HARMON Extra Strength Pain Relieving |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 3.5 mL/100mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63940-100 |
| Labeler Name: | Harmon Stores Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120905 |
| Package NDC: | 63940-100-04 |
| Package Description: | 118 mL in 1 TUBE (63940-100-04) |
| NDC Code | 63940-100-04 |
| Proprietary Name | HARMON Extra Strength Pain Relieving |
| Package Description | 118 mL in 1 TUBE (63940-100-04) |
| Product NDC | 63940-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120905 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Harmon Stores Inc. |
| Substance Name | MENTHOL |
| Strength Number | 3.5 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |