Product NDC: | 14783-435 |
Proprietary Name: | LBEL |
Non Proprietary Name: | Aluminum Sesquichlorohydrate |
Active Ingredient(s): | .18 g/mL & nbsp; Aluminum Sesquichlorohydrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 14783-435 |
Labeler Name: | Ventura International Ltd |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part350 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120120 |
Package NDC: | 14783-435-01 |
Package Description: | 50 mL in 1 BOTTLE, PLASTIC (14783-435-01) |
NDC Code | 14783-435-01 |
Proprietary Name | LBEL |
Package Description | 50 mL in 1 BOTTLE, PLASTIC (14783-435-01) |
Product NDC | 14783-435 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Aluminum Sesquichlorohydrate |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120120 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Ventura International Ltd |
Substance Name | ALUMINUM SESQUICHLOROHYDRATE |
Strength Number | .18 |
Strength Unit | g/mL |
Pharmaceutical Classes |