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NUMOTIZINE
NUMOTIZINE - 10546-100-35 - (MENTHOL)
Drug Information of NUMOTIZINE
| Product NDC: | 10546-100 |
| Proprietary Name: | NUMOTIZINE |
| Non Proprietary Name: | MENTHOL |
| Active Ingredient(s): | 1.25 g/100g & nbsp; MENTHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NUMOTIZINE
| Product NDC: | 10546-100 |
| Labeler Name: | Hobart Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111130 |
Package Information of NUMOTIZINE
| Package NDC: | 10546-100-35 |
| Package Description: | 99 g in 1 JAR (10546-100-35) |
NDC Information of NUMOTIZINE
| NDC Code | 10546-100-35 |
| Proprietary Name | NUMOTIZINE |
| Package Description | 99 g in 1 JAR (10546-100-35) |
| Product NDC | 10546-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MENTHOL |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111130 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Hobart Laboratories, Inc. |
| Substance Name | MENTHOL |
| Strength Number | 1.25 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
