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Keralyt
Keralyt - 11086-030-41 - (salicylic acid)
Drug Information of Keralyt
| Product NDC: | 11086-030 |
| Proprietary Name: | Keralyt |
| Non Proprietary Name: | salicylic acid |
| Active Ingredient(s): | 6 g/100g & nbsp; salicylic acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Keralyt
| Product NDC: | 11086-030 |
| Labeler Name: | Summers Laboratories Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091101 |
Package Information of Keralyt
| Package NDC: | 11086-030-41 |
| Package Description: | 1 TUBE in 1 PACKAGE (11086-030-41) > 40 g in 1 TUBE (11086-030-40) |
NDC Information of Keralyt
| NDC Code | 11086-030-41 |
| Proprietary Name | Keralyt |
| Package Description | 1 TUBE in 1 PACKAGE (11086-030-41) > 40 g in 1 TUBE (11086-030-40) |
| Product NDC | 11086-030 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | salicylic acid |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Summers Laboratories Inc |
| Substance Name | SALICYLIC ACID |
| Strength Number | 6 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
