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dynaFreeze
dynaFreeze - 59316-301-10 - (MENTHOL)
Drug Information of dynaFreeze
| Product NDC: | 59316-301 |
| Proprietary Name: | dynaFreeze |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 35 mg/mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of dynaFreeze
| Product NDC: | 59316-301 |
| Labeler Name: | Performance Health LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100825 |
Package Information of dynaFreeze
| Package NDC: | 59316-301-10 |
| Package Description: | 118 mL in 1 TUBE (59316-301-10) |
NDC Information of dynaFreeze
| NDC Code | 59316-301-10 |
| Proprietary Name | dynaFreeze |
| Package Description | 118 mL in 1 TUBE (59316-301-10) |
| Product NDC | 59316-301 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100825 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Performance Health LLC |
| Substance Name | MENTHOL |
| Strength Number | 35 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
