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Biofreeze
Biofreeze - 59316-101-25 - (Menthol)
Drug Information of Biofreeze
| Product NDC: | 59316-101 |
| Proprietary Name: | Biofreeze |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 35 mg/mL & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Biofreeze
| Product NDC: | 59316-101 |
| Labeler Name: | Performance Health Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101103 |
Package Information of Biofreeze
| Package NDC: | 59316-101-25 |
| Package Description: | 118 mL in 1 TUBE, WITH APPLICATOR (59316-101-25) |
NDC Information of Biofreeze
| NDC Code | 59316-101-25 |
| Proprietary Name | Biofreeze |
| Package Description | 118 mL in 1 TUBE, WITH APPLICATOR (59316-101-25) |
| Product NDC | 59316-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20101103 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Performance Health Inc. |
| Substance Name | MENTHOL |
| Strength Number | 35 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
