Sani Professional Brand Sani-Hands description, usages, side effects, indications, overdosage, supplying and lots more!

Sani Professional Brand Sani-Hands

Professional Disposables International, 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
SANI PROFESSIONAL BRAND SANI-HANDS

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Uses


  • For hand washing to decrease bacteria on the skin.
  • Recommended for repeated use.
  • Dries in seconds.

Warnings

  • Flammable, keep away from fire or flame.
  • For external use only.
  • Do not use in or contact the eyes.
  • Discontinue use if irritation and redness develop. If condition persist for more than 72 hours consult a physician.
  • If swallowed, get medical help or contact a Poison Control Center immediately.
  • Keep this out of reach of children unless under adult supervision.

Directions


  • Tear open packet
  • Open and unfold wipe. Thoroughly wipe hands, fingers and wrists. Be sure to utilize the entire wipe. For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe.
  • Discard after single use.

Other information

Dosage


Inactive ingredients

Water, Propylene Glycol, Glycerin, Carbomer, Aminometyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

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Principal Display Panel - 1000 Packets per Case

Sani Professional Brand

SANI-HANDS(R)

  • Kills 99.99% of Germs
  • Removes Soil and Bacteria More Effective Than Gels Alone
  • Contains Moisturizing Aloe and Vitamin E







Packet Label
Principal Display Panel - 1000 Packets per CaseCase Label
Principal Display Panel - 1000 Packets per Case

Active ingredient

Alcohol 65.9% by volume

Purpose

Antiseptic

Sani Professional Brand Sani-Hands

Alcohol CLOTH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10819-6000
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 0.659 mL

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
GLYCERIN
CARBOMER HOMOPOLYMER TYPE C
AMINOMETHYL PROPANEDIOL
Aloe Vera Leaf
ALPHA-TOCOPHEROL ACETATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10819-6000-1 1000 in 1 CASE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2010-05-25


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