Product NDC: | 63940-150 |
Proprietary Name: | HARMON Extra Strength Pain Relieving Roll-On |
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: | 63940-150 |
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: | 63940-150-03 |
Package Description: | 89 mL in 1 BOTTLE, WITH APPLICATOR (63940-150-03) |
NDC Code | 63940-150-03 |
Proprietary Name | HARMON Extra Strength Pain Relieving Roll-On |
Package Description | 89 mL in 1 BOTTLE, WITH APPLICATOR (63940-150-03) |
Product NDC | 63940-150 |
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 |