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Dermarest
Dermarest - 63736-302-24 - (Salicylic Acid)
Drug Information of Dermarest
| Product NDC: | 63736-302 |
| Proprietary Name: | Dermarest |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 7.08 mL/236mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dermarest
| Product NDC: | 63736-302 |
| Labeler Name: | Insight Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100723 |
Package Information of Dermarest
| Package NDC: | 63736-302-24 |
| Package Description: | 1 BOTTLE in 1 CARTON (63736-302-24) > 236 mL in 1 BOTTLE |
NDC Information of Dermarest
| NDC Code | 63736-302-24 |
| Proprietary Name | Dermarest |
| Package Description | 1 BOTTLE in 1 CARTON (63736-302-24) > 236 mL in 1 BOTTLE |
| Product NDC | 63736-302 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100723 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Insight Pharmaceuticals LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | 7.08 |
| Strength Unit | mL/236mL |
| Pharmaceutical Classes |
