SANIGUARD-SF- alcohol liquid 
Inopak. Ltd

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.

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Inopak SaniGuard-SF

Drug Facts

Active ingredient

Alcohol 70% v/v

Purpose

Antiseptic

Uses

Warnings

For external use only.

FLAMMABLE, keep away from heat or flames.

When using this product keep away from eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation and redness develop or if condition persists for more than 72 hours.

Keep out of reach of children. If swallowed, contact a physician or poison control center.

Directions

Inactive ingredients Water, PEG-10 Dimethicone, Glycerin, Isopropyl Myristate, Polyquaternium-11, Disodium EDTA, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate

Manufacturd for

Inopak, LTD. Ringwood, NJ 07456 • 1-800-762-7725 • www.inopak.com

SaniGuard SF

foam hand sanitizer

alcohol 70%

Compliant with CDC Hand Hygiene Guidlines

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

NET CONTENTS: 33.8 FL. OZ. (1000 ML)

58575-150 SaniGuard HS-0622

SANIGUARD-SF 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58575-150
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
POLYQUATERNIUM-11 (1000000 MW) (UNII: 0B44BS5IJS)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58575-150-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/201104/20/2021
2NDC:58575-150-80800 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2011
3NDC:58575-150-101000 mL in 1 BAG; Type 0: Not a Combination Product05/01/201104/20/2021
4NDC:58575-150-121250 mL in 1 BAG; Type 0: Not a Combination Product05/01/201104/20/2021
5NDC:58575-150-373840 mL in 1 BAG; Type 0: Not a Combination Product05/01/201104/20/2021
6NDC:58575-150-18540 mL in 1 BOTTLE; Type 0: Not a Combination Product05/01/2011
7NDC:58575-150-0350 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2021
8NDC:58575-150-011000 mL in 1 POUCH; Type 0: Not a Combination Product04/20/2021
9NDC:58575-150-423800 mL in 1 BOTTLE; Type 0: Not a Combination Product04/20/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/01/2011
Labeler - Inopak. Ltd (194718243)

Revised: 6/2022
Document Id: e2ae02d1-6f7e-4192-e053-2a95a90aa3be
Set id: f05b8a05-1eb8-4734-90e0-9948e685854c
Version: 6
Effective Time: 20220630
 
Inopak. Ltd