Home
>
National Drug Code (NDC)
>
Breakout Control
Breakout Control - 49825-129-02 - (Benzoyl Peroxide)
Drug Information of Breakout Control
| Product NDC: | 49825-129 |
| Proprietary Name: | Breakout Control |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 5 g/100mL & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Breakout Control
| Product NDC: | 49825-129 |
| Labeler Name: | Bioelements, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130614 |
Package Information of Breakout Control
| Package NDC: | 49825-129-02 |
| Package Description: | 1 BOTTLE in 1 CARTON (49825-129-02) > 29 mL in 1 BOTTLE (49825-129-01) |
NDC Information of Breakout Control
| NDC Code | 49825-129-02 |
| Proprietary Name | Breakout Control |
| Package Description | 1 BOTTLE in 1 CARTON (49825-129-02) > 29 mL in 1 BOTTLE (49825-129-01) |
| Product NDC | 49825-129 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130614 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bioelements, Inc. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
