BabyGanics Alcohol Free Foaming Hand Sanitizer description, usages, side effects, indications, overdosage, supplying and lots more!

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BabyGanics Alcohol Free Foaming Hand Sanitizer

KAS Direct LLC dba BabyGanics

BabyGanics Alcohol Free Foaming Hand SanitizerLiquid


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

BabyGanics Alcohol Free Foaming Hand Sanitizer Uses

  • for hand sanitizing to decrease bacteria on the skin
  • recommended for repeated use

Warnings

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Carefully pour product directly into empty BabyGanics Alcohol Free Foaming Hand Sanitizer bottle
  • Important - Fill each bottle only 2/3 full to allow foaming pump to dispense properly
  • Affix foaming pump on bottle and tighten securely

Inactive ingredients

water, cetrimonium chloride, laurtrimonium chloride, dihydroxyethyl cocamine oxide, glycereth-17 cocoate

Dist. by:
KAS Direct, LLC.
Hicksville, NY 11801

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

eco-refill

babyganics ®

alcohol-free
foaming hand sanitizer

fragrance free ∙ moisturizing formula
non-allergenic ∙ kills 99.9% of germs*
pediatrician & dermatologist tested

no: triclosan, parabens, sulfates,
phthalates, artificial fragrances or dyes

040-10449-01

16 FL OZ (473mL)

BabyGanics Alcohol Free Foaming Hand Sanitizer

BabyGanics Alcohol Free Foaming Hand Sanitizer

BENZALKONIUM CHLORIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59062-1044
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
benzalkonium chloride 0.1 mg

Inactive Ingredients

Ingredient Name Strength
water
CETRIMONIUM CHLORIDE
LAURTRIMONIUM CHLORIDE
dihydroxyethyl cocamine oxide
GLYCERETH-17 COCOATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59062-1044-1 473 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2013-08-15


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Be sure to consult your doctor before taking any medication!
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