Home
>
National Drug Code (NDC)
>
Anti-Bac Concentrate
Anti-Bac Concentrate - 49825-724-02 - (Sulfur)
Drug Information of Anti-Bac Concentrate
| Product NDC: | 49825-724 |
| Proprietary Name: | Anti-Bac Concentrate |
| Non Proprietary Name: | Sulfur |
| Active Ingredient(s): | 5 mL/100mL & nbsp; Sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Bac Concentrate
| Product NDC: | 49825-724 |
| Labeler Name: | Bioelements, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100909 |
Package Information of Anti-Bac Concentrate
| Package NDC: | 49825-724-02 |
| Package Description: | 1 JAR in 1 BOX (49825-724-02) > 14 mL in 1 JAR (49825-724-01) |
NDC Information of Anti-Bac Concentrate
| NDC Code | 49825-724-02 |
| Proprietary Name | Anti-Bac Concentrate |
| Package Description | 1 JAR in 1 BOX (49825-724-02) > 14 mL in 1 JAR (49825-724-01) |
| Product NDC | 49825-724 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sulfur |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100909 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Bioelements, Inc. |
| Substance Name | SULFUR |
| Strength Number | 5 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
