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BLEMISH
BLEMISH - 63550-194-23 - (Benzoyl peroxide)
Drug Information of BLEMISH
| Product NDC: | 63550-194 |
| Proprietary Name: | BLEMISH |
| Non Proprietary Name: | Benzoyl peroxide |
| Active Ingredient(s): | 100 mg/mL & nbsp; Benzoyl peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BLEMISH
| Product NDC: | 63550-194 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101019 |
Package Information of BLEMISH
| Package NDC: | 63550-194-23 |
| Package Description: | 30 mL in 1 BOX (63550-194-23) |
NDC Information of BLEMISH
| NDC Code | 63550-194-23 |
| Proprietary Name | BLEMISH |
| Package Description | 30 mL in 1 BOX (63550-194-23) |
| Product NDC | 63550-194 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl peroxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20101019 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
