MOIST SURE- triclosan liquid MOIST SURE- isopropyl alcohol liquid MOIST SURE- alcohol liquid

Moist SURE by

Drug Labeling and Warnings

Moist SURE by is a Otc medication manufactured, distributed, or labeled by DSHealthcare, Steris Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

62% v/v Ethyl Alcohol

Purposes

Surgical Scrub

Healthcare Personnel Handwash

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)

INGREDIENTS AND APPEARANCE

MOIST SURE 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5720
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	7.5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Hexylene Glycol (UNII: KEH0A3F75J)
Sorbitol (UNII: 506T60A25R)
ETHANOLAMINE (UNII: 5KV86114PT)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	03/06/2006

MOIST SURE 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5727
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sorbitol (UNII: 506T60A25R)
Sodium Chloride (UNII: 451W47IQ8X)
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	01/02/1992

MOIST SURE 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5725
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sorbitol (UNII: 506T60A25R)
Sodium Chloride (UNII: 451W47IQ8X)
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	01/02/1992

MOIST SURE 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5726
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	5 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sorbitol (UNII: 506T60A25R)
Sodium Chloride (UNII: 451W47IQ8X)
Iodopropynyl Butylcarbamate (UNII: 603P14DHEB)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	01/02/1992

MOIST SURE 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5743
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302)	Isopropyl Alcohol	630 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Methylpropanediol (UNII: N8F53B3R4R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Glycerin (UNII: PDC6A3C0OX)
Hydroxypropyl Cellulose (UNII: RFW2ET671P)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	05/01/2004

MOIST SURE 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5741
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302)	Isopropyl Alcohol	630 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Methylpropanediol (UNII: N8F53B3R4R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Glycerin (UNII: PDC6A3C0OX)
Hydroxypropyl Cellulose (UNII: RFW2ET671P)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	05/01/2004

MOIST SURE 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5742
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302)	Isopropyl Alcohol	630 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Methylpropanediol (UNII: N8F53B3R4R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Glycerin (UNII: PDC6A3C0OX)
Hydroxypropyl Cellulose (UNII: RFW2ET671P)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	05/01/2004

MOIST SURE 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5740
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302)	Isopropyl Alcohol	630 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Methylpropanediol (UNII: N8F53B3R4R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Glycerin (UNII: PDC6A3C0OX)
Hydroxypropyl Cellulose (UNII: RFW2ET671P)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	05/01/2004

MOIST SURE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5750
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	620 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isobutane (UNII: BXR49TP611)
Sodium Benzoate (UNII: OJ245FE5EU)
Propane (UNII: T75W9911L6)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	01/02/1988

MOIST SURE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0699-5751
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M)	Alcohol	620 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Isobutane (UNII: BXR49TP611)
Sodium Benzoate (UNII: OJ245FE5EU)
Propane (UNII: T75W9911L6)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333E	01/02/1988

Labeler - DSHealthcare (056296981)

Registrant - Steris Corporation (139424188)

Establishment
Name	Address	ID/FEI	Business Operations
Steris Corporation		139424188	MANUFACTURE