Home
>
National Drug Code (NDC)
>
OXY
OXY - 10742-8236-1 - (Salicylic Acid)
Drug Information of OXY
| Product NDC: | 10742-8236 |
| Proprietary Name: | OXY |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 20 mg/mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OXY
| Product NDC: | 10742-8236 |
| Labeler Name: | The Mentholatum Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100802 |
Package Information of OXY
| Package NDC: | 10742-8236-1 |
| Package Description: | 295 mL in 1 BOTTLE (10742-8236-1) |
NDC Information of OXY
| NDC Code | 10742-8236-1 |
| Proprietary Name | OXY |
| Package Description | 295 mL in 1 BOTTLE (10742-8236-1) |
| Product NDC | 10742-8236 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100802 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | The Mentholatum Company |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
