Home
>
National Drug Code (NDC)
>
Anti-Blemish
Anti-Blemish - 63550-154-90 - (Salicylic Acid)
Drug Information of Anti-Blemish
| Product NDC: | 63550-154 |
| Proprietary Name: | Anti-Blemish |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 20 mg/1 & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | DISC |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Blemish
| Product NDC: | 63550-154 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100809 |
Package Information of Anti-Blemish
| Package NDC: | 63550-154-90 |
| Package Description: | 35 DISC in 1 BOX (63550-154-90) |
NDC Information of Anti-Blemish
| NDC Code | 63550-154-90 |
| Proprietary Name | Anti-Blemish |
| Package Description | 35 DISC in 1 BOX (63550-154-90) |
| Product NDC | 63550-154 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | DISC |
| Route Name | TOPICAL |
| Start Marketing Date | 20100809 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
