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Aetna Callus Remover
Aetna Callus Remover - 43345-003-03 - (Salicylic Acid)
Drug Information of Aetna Callus Remover
| Product NDC: | 43345-003 |
| Proprietary Name: | Aetna Callus Remover |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | .4 1/1001 & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PLASTER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aetna Callus Remover
| Product NDC: | 43345-003 |
| Labeler Name: | Aetna Felt Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19951031 |
Package Information of Aetna Callus Remover
| Package NDC: | 43345-003-03 |
| Package Description: | 4 PLASTER in 1 PACKET (43345-003-03) |
NDC Information of Aetna Callus Remover
| NDC Code | 43345-003-03 |
| Proprietary Name | Aetna Callus Remover |
| Package Description | 4 PLASTER in 1 PACKET (43345-003-03) |
| Product NDC | 43345-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | PLASTER |
| Route Name | TOPICAL |
| Start Marketing Date | 19951031 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Aetna Felt Corp |
| Substance Name | SALICYLIC ACID |
| Strength Number | .4 |
| Strength Unit | 1/1001 |
| Pharmaceutical Classes |
