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ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer
ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer - 49765-310-01 - (BENZALKONIUM CHLORIDE)
Drug Information of ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer
| Product NDC: | 49765-310 |
| Proprietary Name: | ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer |
| 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 ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer
| Product NDC: | 49765-310 |
| Labeler Name: | Artemis Bio-Solutions Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110224 |
Package Information of ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer
| Package NDC: | 49765-310-01 |
| Package Description: | 50 mL in 1 BOTTLE (49765-310-01) |
NDC Information of ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer
| NDC Code | 49765-310-01 |
| Proprietary Name | ARTEMIS Alcohol-Free Antiseptic Foam Hand Sanitizer |
| Package Description | 50 mL in 1 BOTTLE (49765-310-01) |
| Product NDC | 49765-310 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20110224 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Artemis Bio-Solutions Inc |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .13 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
