Clario Free Foaming Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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Clario Free Foaming Hand Sanitizer

Betco corporation, Ltd.
Betco corporation, Ltd.

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert

Clario Free Foaming Hand Sanitizer


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Clario Free Foaming Hand Sanitizer

​Active Ingredient

Benzalkonium Chloride 0.13%

Clario Free Foaming Hand Sanitizer

Uses

  • Use in a variety of public facilities.
  • Use this product when soap and water are not available.

Clario Free Foaming Hand Sanitizer

Warnings

  • For external use only.
  • Avoid contact with eyes.
  • Children under the age of 6 should be supervised by an adult when using this product.
  • Discontinue use is irritation or redness develops.
  • If irritation persists for more than 72 hours, consult a physician.
  • KEEP OUT OF REACH OF CHILDREN.

Clario Free Foaming Hand Sanitizer

Directions

  • ​Read the entire label before using this product.
  • ​Dispense 1-2 pumps of product onto dry hands. Rub hands together to distribute product

Clario Free Foaming Hand Sanitizer

Inactive Ingredients

Deionized ​Water, Sodium PCA, PEG/PPG-8/3 Laurate, Dimethicone, DMDM Hydantoin, PEG-3 Cocamide, Fragrance, Iodoproynyl Btylcarbamate, D&C Green #5.

Clario Free Foaming Hand Sanitizer

Questions or Comments? Phone: (800) 777-9343

MDS information: ​(800) 891-4965

Clario Free Foaming Hand Sanitizer

Purpose

Antiseptic

Clario Free Foaming Hand Sanitizer

KEEP OUT OF REACH OF CHILDREN

Clario Free Foaming Hand Sanitizer

Clario Free Foaming Hand Sanitizer

Nonalcohol Hand Sanitizer

Clario Free Foaming Hand Sanitizer

Clario Free Foaming Hand Sanitizer

Benzalkonium Chloride SOAP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65601-778
Route of Administration Topical DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 1.3 mg

Inactive Ingredients

Ingredient Name Strength
water
SODIUM PYRROLIDONE CARBOXYLATE
polyethylene glycol 400
DIMETHICONE
DMDM HYDANTOIN
PEG-6 COCAMIDE
IODOPROPYNYL BUTYLCARBAMATE
D&C GREEN NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65601-778-53 50 in 1 BOTTLE, PUMP
2 NDC:65601-778-29 1000 in 1 BAG
3 NDC:65601-778-57 550 in 1 BOTTLE, PUMP

Marketing Information

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


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