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ACPURIS
ACPURIS - 52797-020-01 - (SALICYLIC ACID)
Drug Information of ACPURIS
| Product NDC: | 52797-020 |
| Proprietary Name: | ACPURIS |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | .3 mL/15mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ACPURIS
| Product NDC: | 52797-020 |
| Labeler Name: | MEDIWAY KOREA CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of ACPURIS
| Package NDC: | 52797-020-01 |
| Package Description: | 15 mL in 1 CARTON (52797-020-01) |
NDC Information of ACPURIS
| NDC Code | 52797-020-01 |
| Proprietary Name | ACPURIS |
| Package Description | 15 mL in 1 CARTON (52797-020-01) |
| Product NDC | 52797-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | CREAM |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MEDIWAY KOREA CO., LTD. |
| Substance Name | SALICYLIC ACID |
| Strength Number | .3 |
| Strength Unit | mL/15mL |
| Pharmaceutical Classes |
