Product NDC: | 63736-293 |
Proprietary Name: | Skin Shield |
Non Proprietary Name: | Benzethonium Chloride and Dyclonine Hydrochloride |
Active Ingredient(s): | .0532; .0997 mL/27mL; mL/27mL & nbsp; Benzethonium Chloride and Dyclonine Hydrochloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63736-293 |
Labeler Name: | Insight Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 63736-293-24 |
Package Description: | 24 BOX in 1 CASE (63736-293-24) > 1 BOTTLE in 1 BOX > 26.9 mL in 1 BOTTLE |
NDC Code | 63736-293-24 |
Proprietary Name | Skin Shield |
Package Description | 24 BOX in 1 CASE (63736-293-24) > 1 BOTTLE in 1 BOX > 26.9 mL in 1 BOTTLE |
Product NDC | 63736-293 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzethonium Chloride and Dyclonine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Insight Pharmaceuticals |
Substance Name | BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE |
Strength Number | .0532; .0997 |
Strength Unit | mL/27mL; mL/27mL |
Pharmaceutical Classes |