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HONIBE
HONIBE - 50788-001-02 - (MENTHOL)
Drug Information of HONIBE
| Product NDC: | 50788-001 |
| Proprietary Name: | HONIBE |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 8.6 mg/2.5g & nbsp; MENTHOL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LOZENGE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HONIBE
| Product NDC: | 50788-001 |
| Labeler Name: | Island Abbey Foods Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120530 |
Package Information of HONIBE
| Package NDC: | 50788-001-02 |
| Package Description: | 1 BLISTER PACK in 1 BAG (50788-001-02) > 25 g in 1 BLISTER PACK (50788-001-01) |
NDC Information of HONIBE
| NDC Code | 50788-001-02 |
| Proprietary Name | HONIBE |
| Package Description | 1 BLISTER PACK in 1 BAG (50788-001-02) > 25 g in 1 BLISTER PACK (50788-001-01) |
| Product NDC | 50788-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | LOZENGE |
| Route Name | ORAL |
| Start Marketing Date | 20120530 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Island Abbey Foods Ltd. |
| Substance Name | MENTHOL |
| Strength Number | 8.6 |
| Strength Unit | mg/2.5g |
| Pharmaceutical Classes |
