| Product NDC: | 50421-002 |
| Proprietary Name: | Camphor, Menthol |
| Non Proprietary Name: | Camphor, Menthol |
| Active Ingredient(s): | 3.4; 8.5 g/85g; g/85g & nbsp; Camphor, Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50421-002 |
| Labeler Name: | Active & Innovative Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100113 |
| Package NDC: | 50421-002-13 |
| Package Description: | 85 g in 1 BOTTLE, WITH APPLICATOR (50421-002-13) |
| NDC Code | 50421-002-13 |
| Proprietary Name | Camphor, Menthol |
| Package Description | 85 g in 1 BOTTLE, WITH APPLICATOR (50421-002-13) |
| Product NDC | 50421-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Camphor, Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100113 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Active & Innovative Inc. |
| Substance Name | CAMPHOR; MENTHOL |
| Strength Number | 3.4; 8.5 |
| Strength Unit | g/85g; g/85g |
| Pharmaceutical Classes |