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Urea
Urea - 58980-608-80 - (Urea)
Drug Information of Urea
| Product NDC: | 58980-608 |
| Proprietary Name: | Urea |
| Non Proprietary Name: | Urea |
| Active Ingredient(s): | 1 mL/10mL & nbsp; Urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Urea
| Product NDC: | 58980-608 |
| Labeler Name: | Stratus Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100520 |
Package Information of Urea
| Package NDC: | 58980-608-80 |
| Package Description: | 1 BOTTLE in 1 BOX (58980-608-80) > 236.56 mL in 1 BOTTLE |
NDC Information of Urea
| NDC Code | 58980-608-80 |
| Proprietary Name | Urea |
| Package Description | 1 BOTTLE in 1 BOX (58980-608-80) > 236.56 mL in 1 BOTTLE |
| Product NDC | 58980-608 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Urea |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100520 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Stratus Pharmaceuticals, Inc |
| Substance Name | UREA |
| Strength Number | 1 |
| Strength Unit | mL/10mL |
| Pharmaceutical Classes |
