Soft Care Foaming Instant Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

Soft Care Foaming Instant Hand Sanitizer

Diversey, Inc.

  • 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
Drug Facts



FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient

Benzethonium Chloride 0.2%

Purpose

Purpose

Antiseptic handwash

Uses

Uses

For handwashing to decrease bacteria on the skin.

Warnings

Combustible liquid. Keep away from heat, sparks, or flame.

For external use only.

When using this product

Do not use in the eyes. If accidental eye contact occurs, rinse with water.

If eye irritation persists, get medical attention.

Stop use and ask a doctor if irritation and redness develop.

If condition persists for more than 72 hours, consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

To decrease bacteria on skin, apply small amount to palm.

Briskly rub, covering hands with product until dry.

Other information

EMMERGENCY PHONE: 1-800-851-7145

See MSDS #MS0300807

See container for Lot Code and Expiry Date

For Commercial and Industrial Use Only

Inactive ingredients

Water, Alcohol Denat., Cocamidopropyl Betaine, Propylene Glycol, Phenoxyethanol, PEG-7 Glyceryl Cocoate, Tetrasodium EDTA, Aloe Bardadensis Leaf, Tocopheryl Acetate, Fragrance

Questions or comments?

1-800-558-2332 Monday through Friday 7:30 AM to 5:00 PM Central Standard Time

www.diversey.com

Diversey

NDC:64536-1268-1

Soft Care

Foaming Instant Hand Sanitizer

Net Contents

1 L / 1.06 U.S. Qt

5510245


Soft Care Foaming Instant Hand Sanitizer

Benzethonium Chloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:64536-1268
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzethonium chloride BENZETHONIUM 0.2 mL

Inactive Ingredients

Ingredient Name Strength
water
COCAMIDOPROPYL BETAINE
propylene glycol
PHENOXYETHANOL
EDETATE SODIUM
Aloe Vera Leaf
ALPHA-TOCOPHEROL ACETATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:64536-1268-1 1000 in 1 BAG

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-10-11


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