| 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: | 63736-293-36 |
| Package Description: | 36 BOX in 1 CASE (63736-293-36) > 1 BOTTLE in 1 BOX > 29.6 mL in 1 BOTTLE |
| NDC Code | 63736-293-36 |
| Proprietary Name | Skin Shield |
| Package Description | 36 BOX in 1 CASE (63736-293-36) > 1 BOTTLE in 1 BOX > 29.6 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 |