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Relovox
Relovox - 51350-005-06 - (Renewing Clarifying Cleanser)
Drug Information of Relovox
| Product NDC: | 51350-005 |
| Proprietary Name: | Relovox |
| Non Proprietary Name: | Renewing Clarifying Cleanser |
| Active Ingredient(s): | 25 mg/g & nbsp; Renewing Clarifying Cleanser |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Relovox
| Product NDC: | 51350-005 |
| Labeler Name: | Transdermal Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110331 |
Package Information of Relovox
| Package NDC: | 51350-005-06 |
| Package Description: | 1 TUBE in 1 CARTON (51350-005-06) > 30 g in 1 TUBE (51350-005-05) |
NDC Information of Relovox
| NDC Code | 51350-005-06 |
| Proprietary Name | Relovox |
| Package Description | 1 TUBE in 1 CARTON (51350-005-06) > 30 g in 1 TUBE (51350-005-05) |
| Product NDC | 51350-005 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Renewing Clarifying Cleanser |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110331 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Transdermal Corp |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
