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Mineral Ice
Mineral Ice - 0067-2067-16 - (Menthol)
Drug Information of Mineral Ice
| Product NDC: | 0067-2067 |
| Proprietary Name: | Mineral Ice |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | .02 g/g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mineral Ice
| Product NDC: | 0067-2067 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111101 |
Package Information of Mineral Ice
| Package NDC: | 0067-2067-16 |
| Package Description: | 453.6 g in 1 JAR (0067-2067-16) |
NDC Information of Mineral Ice
| NDC Code | 0067-2067-16 |
| Proprietary Name | Mineral Ice |
| Package Description | 453.6 g in 1 JAR (0067-2067-16) |
| Product NDC | 0067-2067 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20111101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | MENTHOL |
| Strength Number | .02 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
