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SE BPO
SE BPO - 13925-121-10 - (Benzoyl Peroxide)
Drug Information of SE BPO
| Product NDC: | 13925-121 |
| Proprietary Name: | SE BPO |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | & nbsp; Benzoyl Peroxide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SE BPO
| Product NDC: | 13925-121 |
| Labeler Name: | Seton Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101004 |
Package Information of SE BPO
| Package NDC: | 13925-121-10 |
| Package Description: | 1 KIT in 1 CARTON (13925-121-10) * 180 g in 1 TUBE * 7 APPLICATOR in 1 CARTON > .5 g in 1 APPLICATOR |
NDC Information of SE BPO
| NDC Code | 13925-121-10 |
| Proprietary Name | SE BPO |
| Package Description | 1 KIT in 1 CARTON (13925-121-10) * 180 g in 1 TUBE * 7 APPLICATOR in 1 CARTON > .5 g in 1 APPLICATOR |
| Product NDC | 13925-121 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20101004 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Seton Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
