HAND SANITIZER- alcohol gel 
Kenher Servicios Industriales, S.de R.L. de C.V.

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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This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (0.2% v/v).
  3. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

glycerin, purified water USP

3800 ml label3800mL NDC 76539-111-38

4000 ml label4000 mL NDC 76539-11-40

1000 ml label1000 mL NDC 76539-11-10

550 ml label550 mL NDC 76539-11-40

500 ml label500 mL NDC 76539-11-50

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76539-111
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
GLYCERIN (UNII: PDC6A3C0OX) 0.2 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76539-111-383800 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
2NDC:76539-111-404000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
3NDC:76539-111-101000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
4NDC:76539-111-50500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
5NDC:76539-111-55550 mL in 1 BOTTLE; Type 0: Not a Combination Product03/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/30/2020
Labeler - Kenher Servicios Industriales, S.de R.L. de C.V. (951576728)
Establishment
NameAddressID/FEIBusiness Operations
Kenher Servicios Industriales, S.de R.L. de C.V.951576728manufacture(76539-111)

Revised: 4/2020
Document Id: a463120f-4df4-268d-e053-2995a90ac508
Set id: a462fc18-8669-1430-e053-2995a90a4cbb
Version: 2
Effective Time: 20200428
 
Kenher Servicios Industriales, S.de R.L. de C.V.