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SALICYLIC ACID
SALICYLIC ACID - 13925-050-01 - (SALICYLIC ACID)
Drug Information of SALICYLIC ACID
| Product NDC: | 13925-050 |
| Proprietary Name: | SALICYLIC ACID |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | & nbsp; SALICYLIC ACID |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SALICYLIC ACID
| Product NDC: | 13925-050 |
| Labeler Name: | Seton Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081101 |
Package Information of SALICYLIC ACID
| Package NDC: | 13925-050-01 |
| Package Description: | 1 KIT in 1 CARTON (13925-050-01) * 237 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON > 355 mL in 1 BOTTLE |
NDC Information of SALICYLIC ACID
| NDC Code | 13925-050-01 |
| Proprietary Name | SALICYLIC ACID |
| Package Description | 1 KIT in 1 CARTON (13925-050-01) * 237 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON > 355 mL in 1 BOTTLE |
| Product NDC | 13925-050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20081101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Seton Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
