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Moist SURE

DSHealthcare
STERIS Corporation

Moist SURE™ Foaming Sanitizer


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

62% v/v Ethyl Alcohol

Purposes

Surgical Scrub

Healthcare Personnel Handwash

Moist SURE Uses

  • Surgical Scrub
  • Healthcare Personnel Handwash in patient care or other high risk settings to reduce transient bacteria and the risk of cross contamination. Use when hands are physically clean.

Warnings

Flammable, keep away from fire or flame. For external use only. Avoid contact with eyes. Eye irritant. If splashed in eyes, rinse promptly and thoroughly with water. Discontinue use if irritation and redness develop. Keep this and all drugs out of the reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately. Contents under pressure. Do not puncture or incinerate. Do not store above 120°F (49°C). For best foam density store and use at 55 - 85°F (13 - 29°C).

Stop use and ask a doctor if irritation and redness develop and persist for more than 5 days.

Directions

Surgical Scrub Clean under nails with a pick. Nails should be maintained with a 1 mm free edge. Dispense 5 grams (tennis ball) onto one hand. Spread on both hands, paying particular attention to the nails, cuticles, and interdigital spaces and forearms. Rub into skin until dry. Dispense 2.5 grams (golf ball) onto one hand and spread over both hands to the wrists and rub into the skin until dry. Healthcare Personnel Handwash Dispense a palm full (golf ball) in one hand. Spread over both hands up to one-half inch above the wrists. Rub vigorously.

Inactive ingredients

Water, Hydrofluorocarbon 152A, Isobutane, Emulsifying Wax, Polyquaternium-6, Sodium Benzoate, Propane, Sodium Sesquicarbonate

Questions or comments?

800-637-8582 • 201-871-1232

PRINCIPAL DISPLAY PANEL - 62.4 g Label

NDC 0699-5750-76

Foaming Sanitizer

Moist
SURE

  • Increased skin hydration
    for up to 2 hours
  • Effective against
    MRSA in 5 seconds
  • Surgical scrub

REF95750
Net Weight: 2.2 oz [62.4 g]

Manufactured for:

Sultan ®

Sultan Healthcare

411 Hackensack Avenue, 9th Floor • Hackensack, NJ 07601
Toll Free: 800-637-8582 • Phone: 201-871-1232
Fax: 201-871-0321 • www.sultanhealthcare.com

62164
10D5-PSB(1209)

Moist SURE

Moist SURE

Triclosan LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5720
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 7.5 mg

Inactive Ingredients

Ingredient Name Strength
water
Hexylene Glycol
sorbitol
ETHANOLAMINE
CITRIC ACID MONOHYDRATE
Ammonium Lauryl Sulfate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5720-13 448 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2006-03-06


Moist SURE

Triclosan LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5727
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 5 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
SODIUM CHLORIDE
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5727-41 1039 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 1992-01-02


Moist SURE

Triclosan LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5725
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 5 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
SODIUM CHLORIDE
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5725-03 123 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 1992-01-02


Moist SURE

Triclosan LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5726
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 5 mg

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
SODIUM CHLORIDE
IODOPROPYNYL BUTYLCARBAMATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5726-13 461 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 1992-01-02


Moist SURE

Isopropyl Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5743
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL 630 mg

Inactive Ingredients

Ingredient Name Strength
water
methylpropanediol
PHENOXYETHANOL
GLYCERIN
hydroxypropyl cellulose

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5743-03 105 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2004-05-01


Moist SURE

Isopropyl Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5741
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL 630 mg

Inactive Ingredients

Ingredient Name Strength
water
methylpropanediol
PHENOXYETHANOL
GLYCERIN
hydroxypropyl cellulose

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5741-13 396 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2004-05-01


Moist SURE

Isopropyl Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5742
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL 630 mg

Inactive Ingredients

Ingredient Name Strength
water
methylpropanediol
PHENOXYETHANOL
GLYCERIN
hydroxypropyl cellulose

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5742-41 891 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2004-05-01


Moist SURE

Isopropyl Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5740
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ISOPROPYL ALCOHOL ISOPROPYL ALCOHOL 630 mg

Inactive Ingredients

Ingredient Name Strength
water
methylpropanediol
PHENOXYETHANOL
GLYCERIN
hydroxypropyl cellulose

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5740-25 53 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2004-05-01


Moist SURE

Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5750
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 620 mg

Inactive Ingredients

Ingredient Name Strength
water
isobutane
SODIUM BENZOATE
propane

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5750-76 62.4 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 1988-01-02


Moist SURE

Alcohol LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0699-5751
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ALCOHOL ALCOHOL 620 mg

Inactive Ingredients

Ingredient Name Strength
water
isobutane
SODIUM BENZOATE
propane

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0699-5751-36 255 in 1 BOTTLE, PUMP

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 1988-01-02


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