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BIOFREEZE
BIOFREEZE - 59316-102-15 - (MENTHOL)
Drug Information of BIOFREEZE
| Product NDC: | 59316-102 |
| Proprietary Name: | BIOFREEZE |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 40 mg/mL & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BIOFREEZE
| Product NDC: | 59316-102 |
| Labeler Name: | Performance Health LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120103 |
Package Information of BIOFREEZE
| Package NDC: | 59316-102-15 |
| Package Description: | 89 mL in 1 BOTTLE, WITH APPLICATOR (59316-102-15) |
NDC Information of BIOFREEZE
| NDC Code | 59316-102-15 |
| Proprietary Name | BIOFREEZE |
| Package Description | 89 mL in 1 BOTTLE, WITH APPLICATOR (59316-102-15) |
| Product NDC | 59316-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120103 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Performance Health LLC |
| Substance Name | MENTHOL |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
