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Elgin Pain Relief
Elgin Pain Relief - 30056-004-32 - (Menthol)
Drug Information of Elgin Pain Relief
| Product NDC: | 30056-004 |
| Proprietary Name: | Elgin Pain Relief |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 35 mg/g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Elgin Pain Relief
| Product NDC: | 30056-004 |
| Labeler Name: | Eco-Logics, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091215 |
Package Information of Elgin Pain Relief
| Package NDC: | 30056-004-32 |
| Package Description: | 877 g in 1 BOTTLE, PUMP (30056-004-32) |
NDC Information of Elgin Pain Relief
| NDC Code | 30056-004-32 |
| Proprietary Name | Elgin Pain Relief |
| Package Description | 877 g in 1 BOTTLE, PUMP (30056-004-32) |
| Product NDC | 30056-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20091215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Eco-Logics, Inc. |
| Substance Name | MENTHOL |
| Strength Number | 35 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
