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Aloquin
Aloquin - 68040-706-16 - (Aloe Vera Leaf and Iodoquinol)
Drug Information of Aloquin
| Product NDC: | 68040-706 |
| Proprietary Name: | Aloquin |
| Non Proprietary Name: | Aloe Vera Leaf and Iodoquinol |
| Active Ingredient(s): | 10; 12.5 mg/g; mg/g & nbsp; Aloe Vera Leaf and Iodoquinol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aloquin
| Product NDC: | 68040-706 |
| Labeler Name: | Primus Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090706 |
Package Information of Aloquin
| Package NDC: | 68040-706-16 |
| Package Description: | 1 TUBE in 1 BOX (68040-706-16) > 60 g in 1 TUBE |
NDC Information of Aloquin
| NDC Code | 68040-706-16 |
| Proprietary Name | Aloquin |
| Package Description | 1 TUBE in 1 BOX (68040-706-16) > 60 g in 1 TUBE |
| Product NDC | 68040-706 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Aloe Vera Leaf and Iodoquinol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20090706 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Primus Pharmaceuticals |
| Substance Name | ALOE VERA LEAF; IODOQUINOL |
| Strength Number | 10; 12.5 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
