MICRELL Antibacterial Foam Handwash description, usages, side effects, indications, overdosage, supplying and lots more!

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MICRELL Antibacterial Foam Handwash

GOJO Industries, Inc.

MICRELL Antibacterial Foam Handwash


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Chloroxylenol 0.5%

Purpose

Antimicrobial

Use

Handwash to help decrease bacteria on the skin

Recommended for repeated use

Warnings

For external use only

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash appears and lasts.

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

Directions

Wet hands.

Apply product and thoroughly cover hands with lather.

Rinse well and dry hands completely.

Inactive ingredients

Water (Aqua), Alcohol, Lauric Acid, Ethanolamine, Dipropylene Glycol, Lactic Acid, Poloxamer 124, Isopropyl Alcohol, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Fragrance (Parfum), Methylparaben, Propylparaben, Green 3 (CI 42053), Red 33 (CI 17200)

Package/Label Principal Display Panel

MICRELL Antibacterial Foam Handwash

Brought to you by GOJO

GOJO Industries, Inc. Akron, OH 44309

Questions? 800-321-9647 • 330-255-6000 www.GOJO.com

©2011. GOJO Industries, Inc.

All rights reserved.

Made in U.S.A.

MICRELL Antibacterial Foam Handwash

MICRELL Antibacterial Foam Handwash

CHLOROXYLENOL LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21749-095
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Chloroxylenol Chloroxylenol 0.005 mg

Inactive Ingredients

Ingredient Name Strength
water
ALCOHOL
Lauric Acid
MONOETHANOLAMINE
DIPROPYLENE GLYCOL
LACTIC ACID
Poloxamer 124
ISOPROPYL ALCOHOL
SODIUM METABISULFITE
SODIUM SULFITE
EDETATE SODIUM
SODIUM SULFATE
METHYLPARABEN
PROPYLPARABEN
FD&C GREEN NO. 3
D&C RED NO. 33

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21749-095-22 200 in 1 BOTTLE
2 NDC:21749-095-53 535 in 1 BOTTLE
3 NDC:21749-095-97 700 in 1 BOTTLE
4 NDC:21749-095-89 1200 in 1 BOTTLE
5 NDC:21749-095-90 1250 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2006-06-23


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Be sure to consult your doctor before taking any medication!
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