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

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Sani-Hands

Professional Disposables International, Inc.

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Sani-Hands 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 right away.
  • Keep this out of reach of children unless under adult supervision.

Directions


  • Tear open pouch
  • 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.

Sani-Hands Other information

Lot No. and Expiration Date can be found on pouch, on packet or on top of carton.

Dosage

For dirty hand, use first wipe to clean hands, then discard wipe; sanitize with second wipe. Discard after single use.

Inactive ingredients

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

*Wipes composed of 50% Tencel,
50% Viscose, both made from renewable resources.
Tencel(R) is a registered trademark of Lenzing AG.

Manufactured for:
Nice-Pak Products, Inc.
Orangeburg, NY 10962-1376 - USA - 1-800-999-6423
Made in USA

Principal Display Panel

Sani
Professional Brand

SANI-HANDS(R)
Instant Hand Sanitizing Wipes

#1 in Hospitals and Doctors' Offices

Clinically Proven More Effective than Gels

Kills 99.99% of Germs

Pouch Label
Sani-Hands
Individual packet
Sani-Hands
Box of 24 packets
Sani-Hands

Active ingredient

Alcohol 65.9% by volume

Purpose

Antiseptic

Sani-Hands

Alcohol CLOTH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10819-5811
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:10819-5811-8 8 in 1 POUCH
2 NDC:10819-5811-9 24 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2012-02-08


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