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InstantFOAM non-alcohol
InstantFOAM non-alcohol - 11084-058-20 - (BENZALKONIUM CHLORIDE)
Drug Information of InstantFOAM non-alcohol
| Product NDC: | 11084-058 |
| Proprietary Name: | InstantFOAM non-alcohol |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .13 mL/100mL & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of InstantFOAM non-alcohol
| Product NDC: | 11084-058 |
| Labeler Name: | Deb USA, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100101 |
Package Information of InstantFOAM non-alcohol
| Package NDC: | 11084-058-20 |
| Package Description: | 2000 mL in 1 BOTTLE, PLASTIC (11084-058-20) |
NDC Information of InstantFOAM non-alcohol
| NDC Code | 11084-058-20 |
| Proprietary Name | InstantFOAM non-alcohol |
| Package Description | 2000 mL in 1 BOTTLE, PLASTIC (11084-058-20) |
| Product NDC | 11084-058 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Deb USA, Inc. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .13 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
