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Unagel
Unagel - 52205-001-00 - (SALICYLIC ACID)
Drug Information of Unagel
| Product NDC: | 52205-001 |
| Proprietary Name: | Unagel |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 2 g/100g & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Unagel
| Product NDC: | 52205-001 |
| Labeler Name: | Advanced Skin Technology, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120904 |
Package Information of Unagel
| Package NDC: | 52205-001-00 |
| Package Description: | 29 g in 1 BOTTLE (52205-001-00) |
NDC Information of Unagel
| NDC Code | 52205-001-00 |
| Proprietary Name | Unagel |
| Package Description | 29 g in 1 BOTTLE (52205-001-00) |
| Product NDC | 52205-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120904 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Advanced Skin Technology, LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
