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SCRUBS Foaming Hand Sanitizer
SCRUBS Foaming Hand Sanitizer - 51239-1929-7 - (Hand Sanitizer Foam)
Drug Information of SCRUBS Foaming Hand Sanitizer
| Product NDC: | 51239-1929 |
| Proprietary Name: | SCRUBS Foaming Hand Sanitizer |
| Non Proprietary Name: | Hand Sanitizer Foam |
| Active Ingredient(s): | .1; .1 g/970mL; g/970mL & nbsp; Hand Sanitizer Foam |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SCRUBS Foaming Hand Sanitizer
| Product NDC: | 51239-1929 |
| Labeler Name: | ITW Dymon |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091001 |
Package Information of SCRUBS Foaming Hand Sanitizer
| Package NDC: | 51239-1929-7 |
| Package Description: | 252 mL in 1 BOTTLE, PUMP (51239-1929-7) |
NDC Information of SCRUBS Foaming Hand Sanitizer
| NDC Code | 51239-1929-7 |
| Proprietary Name | SCRUBS Foaming Hand Sanitizer |
| Package Description | 252 mL in 1 BOTTLE, PUMP (51239-1929-7) |
| Product NDC | 51239-1929 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hand Sanitizer Foam |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091001 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ITW Dymon |
| Substance Name | BENZALKONIUM CHLORIDE; BENZETHONIUM CHLORIDE |
| Strength Number | .1; .1 |
| Strength Unit | g/970mL; g/970mL |
| Pharmaceutical Classes |
