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

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Hand Sanitizer

McKesson
Vi-Jon

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient

Ethyl alcohol 70%

purpose

Antiseptic

Hand Sanitizer Uses

  • to decrease bacteria on the skin that could cause disease
  • recommend for repeated use

Warnings

For external use only-hands

Flammable

Keep away from heat and flame

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

Skin irritation develops

Keep out of reach of children

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

Directions

  • wet hands thoroghly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Hand Sanitizer Other information

  • do not sore above 105⁰ F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

Claims

Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds

SDS-MO-15036  SDA-WI-2486  DSP-MO-28   DSP-MO-34

Disclaimer

Not manufactured or distributed by GOJO industries, Inc.  distributor of Purell Refreshing Gel Advanced Hand Sanitizer

Made in USA with US and foreign components

Side Effects Section

Another Quality Product Distributed By McKesson

One Post Street, San Francisco, CA 94104

Money Back Guarantee

Please visit us at www.sunmarkbrand.com

Principal display panel

sunmark

COMPARE TO PURELL

NDC 49348-405-37

hand

sanitizer

more effective formula

Kills more than 99.99% of germs

ADVANCED

8FL OZ (236 mL)

Hand Sanitizer

Hand Sanitizer

Alcohol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-405
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 70 mL

Inactive Ingredients

Ingredient Name Strength
water
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)
SULISOBENZONE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-405-31 59 in 1 BOTTLE, PLASTIC
2 NDC:49348-405-37 236 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2013-01-21


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