Knuckle Under Medicated description, usages, side effects, indications, overdosage, supplying and lots more!

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Knuckle Under Medicated

Betco corporation, Ltd.
Betco corporation, Ltd.

Knuckle Under Medicated


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Knuckle Under Medicated

​Active Ingredient

​Chloroxylenol 0.5%

Knuckle Under Medicated

Uses

  • ​For use in a variety of industrial setting including manufacturing, machine shops, maintenance areas and automotive shops.

Knuckle Under Medicated

Warnings

  • For external use only.
  • Avoid contact with eyes.
  • If contact occurs, rinse thoroughly with water.
  • Discontinue use is irritation or redness develops.
  • If irritation persists for more than 72 hours, consult a physician.
  • KEEP OUT OF REACH OF CHILDREN.
  • If swallowed, get medical help or contact a poison control center right away.

Knuckle Under Medicated

Directions

  • ​Read the entire label before using this product.
  • ​Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands..
  • Rinse with clean water.

Knuckle Under Medicated

Inactive Ingredients

​Water, Sodium Laureth lSulfate, Tetrasodium EDTA, ethanol, Coco MIPA, Fragrance, sodium chloride, Cocamidopropropyl Betaine, D&C Green #5, FD&C Yellow #5.

Knuckle Under Medicated

Purpose

Antibacterial

Knuckle Under Medicated

KEEP OUT OF REACH OF CHILDREN

Knuckle Under Medicated

Knuckle Under Medicated
HAND CLEANER

Antibacterial Hand Cleaner for Industrial Applications

HAND CLEANER 765

1 Gallon (U.S./E.U.) 3.78 L

Knuckle Under Medicated

Knuckle Under Medicated

Chloroxylenol SOAP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65601-765
Route of Administration Topical DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Chloroxylenol Chloroxylenol 5.0 mg

Inactive Ingredients

Ingredient Name Strength
water
SODIUM LAURETH SULFATE
EDETATE SODIUM
TALL OIL ACID
ALCOHOL
COCO MONOISOPROPANOLAMIDE
SODIUM CHLORIDE
COCAMIDOPROPYL BETAINE
D&C GREEN NO. 5
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65601-765-19 900 in 1 BAG
2 NDC:65601-765-10 1100 in 1 BAG
3 NDC:65601-765-04 3780 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2012-11-12


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Be sure to consult your doctor before taking any medication!
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