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OBLITERATE
OBLITERATE - 49520-101-51 - (BENZOYL PEROXIDE)
Drug Information of OBLITERATE
| Product NDC: | 49520-101 |
| Proprietary Name: | OBLITERATE |
| Non Proprietary Name: | BENZOYL PEROXIDE |
| Active Ingredient(s): | 5 g/100mL & nbsp; BENZOYL PEROXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OBLITERATE
| Product NDC: | 49520-101 |
| Labeler Name: | mybody |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120424 |
Package Information of OBLITERATE
| Package NDC: | 49520-101-51 |
| Package Description: | 1 BOTTLE in 1 BOX (49520-101-51) > 15 mL in 1 BOTTLE (49520-101-11) |
NDC Information of OBLITERATE
| NDC Code | 49520-101-51 |
| Proprietary Name | OBLITERATE |
| Package Description | 1 BOTTLE in 1 BOX (49520-101-51) > 15 mL in 1 BOTTLE (49520-101-11) |
| Product NDC | 49520-101 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZOYL PEROXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120424 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | mybody |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
