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

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Advanced Hand Sanitizer

CVS Pharmacy, Inc
Vi-Jon

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

active ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Advanced Hand Sanitizer Uses

  • to decrease bacteria on the skin that could cause disease
  • recommended 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 thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision
  • not recommended for infants

Advanced Hand Sanitizer Other information

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

Inactive ingredients

water, aloe, barbadensis leaf juice, glyceryl, caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

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

Side Effects

Distributed by:

CVS Pharmacy, Inc

One CVS Drive

Woonsockot, RI 02805

www.cvs.com   1-800-shop-CVS

Made in the U.S.A. with U.S. and foreign components

Principal display panel

CVS

Pharmacy

advanced

formula

hand

sanitizer

with aloe

Kills more than 99.99% of germs

Leaves hands feeling soft

Moisturizing formula

with aloe + vitamin E

32 FL OZ (946 mL)

Advanced Hand Sanitizer

Advanced Hand Sanitizer

Ethyl Alcohol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-070
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 700 mg

Inactive Ingredients

Ingredient Name Strength
water
Aloe Vera Leaf
GLYCERYL CAPRYLATE/CAPRATE
GLYCERIN
ISOPROPYL MYRISTATE
.ALPHA.-TOCOPHEROL ACETATE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
SULISOBENZONE
FD&C BLUE NO. 1
FD&C YELLOW NO. 5

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59779-070-16 59 in 1 BOTTLE, DISPENSING
2 NDC:59779-070-34 236 in 1 BOTTLE, PUMP
3 NDC:59779-070-45 946 in 1 BOTTLE, PUMP
4 NDC:59779-070-26 118 in 1 BOTTLE, PUMP
5 NDC:59779-070-49 443 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partA part333A 2013-10-18


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