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BioFlexor
BioFlexor - 62391-001-04 - (Menthol)
Drug Information of BioFlexor
| Product NDC: | 62391-001 |
| Proprietary Name: | BioFlexor |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | .03 g/g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BioFlexor
| Product NDC: | 62391-001 |
| Labeler Name: | Health Care Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19980301 |
Package Information of BioFlexor
| Package NDC: | 62391-001-04 |
| Package Description: | 135 g in 1 JAR (62391-001-04) |
NDC Information of BioFlexor
| NDC Code | 62391-001-04 |
| Proprietary Name | BioFlexor |
| Package Description | 135 g in 1 JAR (62391-001-04) |
| Product NDC | 62391-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19980301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Health Care Laboratories Inc. |
| Substance Name | MENTHOL |
| Strength Number | .03 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
