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Eucalyptamint
Eucalyptamint - 63736-340-02 - (Menthol)
Drug Information of Eucalyptamint
| Product NDC: | 63736-340 |
| Proprietary Name: | Eucalyptamint |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 9.6 mL/60mL & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Eucalyptamint
| Product NDC: | 63736-340 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090709 |
Package Information of Eucalyptamint
| Package NDC: | 63736-340-02 |
| Package Description: | 1 TUBE in 1 BOX (63736-340-02) > 60 mL in 1 TUBE |
NDC Information of Eucalyptamint
| NDC Code | 63736-340-02 |
| Proprietary Name | Eucalyptamint |
| Package Description | 1 TUBE in 1 BOX (63736-340-02) > 60 mL in 1 TUBE |
| Product NDC | 63736-340 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20090709 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | MENTHOL |
| Strength Number | 9.6 |
| Strength Unit | mL/60mL |
| Pharmaceutical Classes |
