Label: MOIST SURE- triclosan liquid
MOIST SURE- isopropyl alcohol liquid
MOIST SURE- alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 0699-5720-13, 0699-5725-03, 0699-5726-13, 0699-5727-41, view more0699-5740-25, 0699-5741-13, 0699-5742-41, 0699-5743-03, 0699-5750-76, 0699-5751-36 - Packager: DSHealthcare
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 9, 2010
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purposes
- Uses
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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).
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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
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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.com62164
10D5-PSB(1209) -
Increased skin hydration
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INGREDIENTS AND APPEARANCE
MOIST SURE
triclosan liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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 liquidProduct 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