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SaniGuard-SF

Dosage form: liquid
Ingredients: ALCOHOL 70mL in 100mL
Labeler: Inopak. Ltd
NDC Code: 58575-150

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.

SaniGuard-SF

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

SANIGUARD-SF  
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58575-150
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
CHLORHEXIDINE GLUCONATE 
ISOPROPYL ALCOHOL 
PEG-10 DIMETHICONE (600 CST) 
POLYETHYLENE GLYCOL 600000 
PHENOXYETHANOL 
POLYQUATERNIUM-10 (30000 MPA.S AT 2%) 
WATER 
Packaging
#Item CodePackage Description
1NDC:58575-150-0260 mL in 1 BOTTLE
2NDC:58575-150-80800 mL in 1 BOTTLE
3NDC:58575-150-101000 mL in 1 BAG
4NDC:58575-150-121250 mL in 1 BAG
5NDC:58575-150-373840 mL in 1 BAG
6NDC:58575-150-18540 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2011
Labeler - Inopak. Ltd (194718243)
Registrant - Inopak. Ltd (194718243)
Establishment
NameAddressID/FEIOperations
Inopak. Ltd194718243manufacture(58575-150)

 
Inopak. Ltd

Medically reviewed on Nov 1, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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