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TOPCARE
TOPCARE - 36800-235-01 - (ETHYL ALCOHOL)
Drug Information of TOPCARE
| Product NDC: | 36800-235 |
| Proprietary Name: | TOPCARE |
| Non Proprietary Name: | ETHYL ALCOHOL |
| Active Ingredient(s): | 62 mL/100mL & nbsp; ETHYL ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TOPCARE
| Product NDC: | 36800-235 |
| Labeler Name: | TOPCO ASSOCIATES LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111120 |
Package Information of TOPCARE
| Package NDC: | 36800-235-01 |
| Package Description: | 7.4 mL in 1 BOTTLE, SPRAY (36800-235-01) |
NDC Information of TOPCARE
| NDC Code | 36800-235-01 |
| Proprietary Name | TOPCARE |
| Package Description | 7.4 mL in 1 BOTTLE, SPRAY (36800-235-01) |
| Product NDC | 36800-235 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHYL ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20111120 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | TOPCO ASSOCIATES LLC |
| Substance Name | ALCOHOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
