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Proactiv
Proactiv - 11410-812-29 - (SULFUR)
Drug Information of Proactiv
| Product NDC: | 11410-812 |
| Proprietary Name: | Proactiv |
| Non Proprietary Name: | SULFUR |
| Active Ingredient(s): | 6 mg/100mL & nbsp; SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proactiv
| Product NDC: | 11410-812 |
| Labeler Name: | Guthy-Renker LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080201 |
Package Information of Proactiv
| Package NDC: | 11410-812-29 |
| Package Description: | 1 TUBE in 1 BOX (11410-812-29) > 30 mL in 1 TUBE |
NDC Information of Proactiv
| NDC Code | 11410-812-29 |
| Proprietary Name | Proactiv |
| Package Description | 1 TUBE in 1 BOX (11410-812-29) > 30 mL in 1 TUBE |
| Product NDC | 11410-812 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20080201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Guthy-Renker LLC |
| Substance Name | SULFUR |
| Strength Number | 6 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
