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Blue Gel
Blue Gel - 0536-2302-59 - (Menthol)
Drug Information of Blue Gel
| Product NDC: | 0536-2302 |
| Proprietary Name: | Blue Gel |
| 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 Blue Gel
| Product NDC: | 0536-2302 |
| Labeler Name: | Rugby Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121029 |
Package Information of Blue Gel
| Package NDC: | 0536-2302-59 |
| Package Description: | 227 g in 1 JAR (0536-2302-59) |
NDC Information of Blue Gel
| NDC Code | 0536-2302-59 |
| Proprietary Name | Blue Gel |
| Package Description | 227 g in 1 JAR (0536-2302-59) |
| Product NDC | 0536-2302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20121029 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Rugby Laboratories |
| Substance Name | MENTHOL |
| Strength Number | .02 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
