Home – FOAMING HAND SANITIZER
FOAMING HAND SANITIZER
HEB
DRUG FACTS BOX (BACK LABEL)
FULL PRESCRIBING INFORMATION: CONTENTS*
FULL PRESCRIBING INFORMATION
ACTIVE INGREDIENT
BENZALKONIUM CHLORIDE 0.1% (ANTISEPTIC)
USES AND DIRECTIONS
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USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
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DIRECTIONS: PUMP ENOUGH PRODUCT TO YOUR PALM TO THOROUGHLY COVER YOUR HANDS, RUB TOGETHER UNTIL DRY.
WARNINGS
WHEN USING THIS PRODUCT
- AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES WITH WATER.
STOP USE AND ASK A DOCTOR IF
- SKIN IRRITATION OR REDNESS DEVELOPS AND LASTS.
KEEP OUT OF REACH OF CHILDREN
- IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.
PACKAGE FRONT AND BACK LABELS
- 8OZ FRONT AND BACK LABELS: hcf8.jpg
FOAMING HAND SANITIZER
BENZALKONIUM CHLORIDE LIQUID
Product Information
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Product Type
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Human otc drug label |
Item Code (Source)
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NDC:37808-240 |
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Route of Administration
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TOPICAL |
DEA Schedule
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Active Ingredient/Active Moiety
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Ingredient Name
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Basis of Strength
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Strength
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benzalkonium chloride |
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0.1000 mL
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Packaging
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#
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Item Code
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Package Description
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Marketing Start Date
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Marketing End Date
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1 |
NDC:37808-240-08 |
236 in 1 BOTTLE, PUMP |
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Marketing Information
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Marketing Category
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Application Number or Monograph Citation
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Marketing Start Date
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Marketing End Date
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part |
part333 |
2010-07-14 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
