SANIGUARD-SF- alcohol liquid

SaniGuard-SF by

Drug Labeling and Warnings

SaniGuard-SF by is a Otc medication manufactured, distributed, or labeled by Inopak. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Drug Facts

Active Ingredient

Ethyl Alcohol 70% w/w

Purpose

Antiseptic

Keep out of reach of children

Keep out of reach of children.

Uses

• For handwashing to decrease bacteria on the skin after changing diapers, assisting ill persons or before contact with a person under  medical care or treatment.
• Recommended for repeated use.
  

Warnings FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

• For external use only. Keep out of eyes, ears or mouth.
• Discontinue use if irritation occurs.

Directions

• If hands are visibly soiled, wash with soap and water and dry hands.
• Wet hands thoroughly with product, especially the area under the fingernails and allow to dry without rinsing.
  

Inactive Ingredients

benzalkonium chloride, chlorhexidine gluconate, isopropyl alcohol, PEG 10 dimethicone, PEG-14M, phenoxyethanol, polyquaternium 10, water

SaniGuard SF Label

SaniGuard  SF

waterless foam hand sanitizer

Compliant with CDC Hand Hygiene Guidlines
Kills more than 99.99% of germs in 15 seconds

Active: Ethyl Alcohol 70%

Does not contain DEA/MEA, triclosan, parabens, formaldehyde, dyes, fragrance

INOPAK LTD.  1-800-762-7725     50ml

INGREDIENTS AND APPEARANCE

SANIGUARD-SF  
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58575-150
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
POLYETHYLENE GLYCOL 600000 (UNII: 2126FD486L)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58575-150-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2011
2	NDC: 58575-150-80	800 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2011
3	NDC: 58575-150-10	1000 mL in 1 BAG; Type 0: Not a Combination Product	05/01/2011
4	NDC: 58575-150-12	1250 mL in 1 BAG; Type 0: Not a Combination Product	05/01/2011
5	NDC: 58575-150-37	3840 mL in 1 BAG; Type 0: Not a Combination Product	05/01/2011
6	NDC: 58575-150-18	540 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/01/2011

Labeler - Inopak. Ltd (194718243)

Registrant - Inopak. Ltd (194718243)

Establishment
Name	Address	ID/FEI	Business Operations
Inopak. Ltd		194718243	manufacture(58575-150)