Product NDC: | 11410-101 |
Proprietary Name: | Proactiv |
Non Proprietary Name: | SULFUR |
Active Ingredient(s): | 8 mg/100mL & nbsp; SULFUR |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11410-101 |
Labeler Name: | Guthy-Renker LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19981201 |
Package NDC: | 11410-101-04 |
Package Description: | 1 VIAL, PLASTIC in 1 BOX (11410-101-04) > 7.5 mL in 1 VIAL, PLASTIC |
NDC Code | 11410-101-04 |
Proprietary Name | Proactiv |
Package Description | 1 VIAL, PLASTIC in 1 BOX (11410-101-04) > 7.5 mL in 1 VIAL, PLASTIC |
Product NDC | 11410-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SULFUR |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 19981201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Guthy-Renker LLC |
Substance Name | SULFUR |
Strength Number | 8 |
Strength Unit | mg/100mL |
Pharmaceutical Classes |