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Myo-Breathe
Myo-Breathe - 41391-119-12 - (Menthol)
Drug Information of Myo-Breathe
| Product NDC: | 41391-119 |
| Proprietary Name: | Myo-Breathe |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 4000 mg/4mL & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Myo-Breathe
| Product NDC: | 41391-119 |
| Labeler Name: | Myo-Breathe |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090110 |
Package Information of Myo-Breathe
| Package NDC: | 41391-119-12 |
| Package Description: | 118 mL in 1 TUBE (41391-119-12) |
NDC Information of Myo-Breathe
| NDC Code | 41391-119-12 |
| Proprietary Name | Myo-Breathe |
| Package Description | 118 mL in 1 TUBE (41391-119-12) |
| Product NDC | 41391-119 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20090110 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Myo-Breathe |
| Substance Name | MENTHOL |
| Strength Number | 4000 |
| Strength Unit | mg/4mL |
| Pharmaceutical Classes |
