Product NDC: | 10481-0112 |
Proprietary Name: | MONSELS SOLUTION |
Non Proprietary Name: | FERRIC SUBSULFATE |
Active Ingredient(s): | .21 g/g & nbsp; FERRIC SUBSULFATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10481-0112 |
Labeler Name: | Gordon Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20100209 |
Package NDC: | 10481-0112-2 |
Package Description: | 59 g in 1 BOTTLE, GLASS (10481-0112-2) |
NDC Code | 10481-0112-2 |
Proprietary Name | MONSELS SOLUTION |
Package Description | 59 g in 1 BOTTLE, GLASS (10481-0112-2) |
Product NDC | 10481-0112 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FERRIC SUBSULFATE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100209 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Gordon Laboratories |
Substance Name | FERRIC SUBSULFATE |
Strength Number | .21 |
Strength Unit | g/g |
Pharmaceutical Classes |