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Azuro
Azuro - 49955-100-10 - (ALCOHOL)
Drug Information of Azuro
| Product NDC: | 49955-100 |
| Proprietary Name: | Azuro |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 L/L & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azuro
| Product NDC: | 49955-100 |
| Labeler Name: | Noveko Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091118 |
Package Information of Azuro
| Package NDC: | 49955-100-10 |
| Package Description: | 1 L in 1 BOTTLE (49955-100-10) |
NDC Information of Azuro
| NDC Code | 49955-100-10 |
| Proprietary Name | Azuro |
| Package Description | 1 L in 1 BOTTLE (49955-100-10) |
| Product NDC | 49955-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20091118 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Noveko Inc |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | L/L |
| Pharmaceutical Classes |
