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SALICYLIC ACID
SALICYLIC ACID - 42192-135-10 - (SALICYLIC ACID)
Drug Information of SALICYLIC ACID
| Product NDC: | 42192-135 |
| Proprietary Name: | SALICYLIC ACID |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 275 mg/mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SALICYLIC ACID
| Product NDC: | 42192-135 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110921 |
Package Information of SALICYLIC ACID
| Package NDC: | 42192-135-10 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (42192-135-10) > 10 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of SALICYLIC ACID
| NDC Code | 42192-135-10 |
| Proprietary Name | SALICYLIC ACID |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (42192-135-10) > 10 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 42192-135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110921 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | 275 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
