FOAMING HAND SANITIZER description, usages, side effects, indications, overdosage, supplying and lots more!

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FOAMING HAND SANITIZER

APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS BOX (BACK LABEL)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE  0.1% (ANTISEPTIC)

USES AND DIRECTIONS

  • USES: TO HELP REDUCE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE. RECOMMENDED FOR REPEATED USE.
  • DIRECTIONS: PUMP DESIRED AMOUNT ONTO HANDS AND RUB UNTIL YOUR SKIN IS DRY. CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

WARNINGS

  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

  • AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. AVOID CONTACT WITH BROKEN SKIN.

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: nc08.jpgFOAMING HAND SANITIZER

FOAMING HAND SANITIZER

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63148-240
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.1000 mL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63148-240-08 236 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part333 2010-06-25


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Be sure to consult your doctor before taking any medication!
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