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

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PROVON Antibacterial Foam Handwash

GOJO Industries, Inc.

PROVON Antibacterial Foam Handwash


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Triclosan 0.3%

Purpose

Antimicrobial

Use

  • Handwash to help decrease bacteria on the skin before and after contact with a person under medical care or treatment
  • 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 a small amount of product and work into a lather
  • Rinse well and dry hands completely

Inactive ingredients

Water (Aqua), Propylene Glycol, Alcohol, Lauric Acid, Ethanolamine, Disodium Cocoamphodiacetate, Lactic Acid, Isopropyl Alcohol, PEG-4, Polyquaternium-10, Sodium Metabisulfite, Sodium Sulfite, Tetrasodium EDTA, Sodium Sulfate, Iodopropynyl Butylcarbamate

Package/Label Principal Display Panel

PROVON Antibacterial Foam Handwash

PROVON Antibacterial Foam Handwash

Triclosan LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21749-533
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 0.003 mg

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
ALCOHOL
Lauric Acid
MONOETHANOLAMINE
DISODIUM COCOAMPHODIACETATE
LACTIC ACID
ISOPROPYL ALCOHOL
POLYETHYLENE GLYCOL 200
POLYQUATERNIUM-10 (30000 MPA.S AT 2%)
SODIUM METABISULFITE
SODIUM SULFITE
EDETATE SODIUM
SODIUM SULFATE
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21749-533-89 1200 in 1 BOTTLE
2 NDC:21749-533-90 1250 in 1 BOTTLE
3 NDC:21749-533-97 700 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2013-01-01


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