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
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.jpg
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 |
|
|