TAVOS HAND SANITIZER GEL- isopropyl alcohol gel 
Tavos Industries Inc.

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. Isopropyl Alcohol (75%, v/v) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (1.45% v/v).
  3. Hydrogen peroxide (0.125% v/v).
  4. 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)

Isopropyl Alcohol 72% 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

carbopol, glycerin, aminomethylpropanol, distilled water

Package Label - Principal Display Panel

Single Use Label187.5 ml NDC: 80234-9009-02

50mL Label

50 ml NDC: 80234-9009-03

250mL Label

250 ml NDC: 80234-9009-04

500mL Label

250 ml NDC: 80234-9009-05

1L Label

250 ml NDC: 80234-9009-06

1G Label

250 ml NDC: 80234-9009-07

TAVOS HAND SANITIZER GEL 
isopropyl alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80234-9009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL72 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX) 1 mL  in 100 mL
WATER (UNII: 059QF0KO0R) 27 mL  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80234-9009-2187.5 mL in 1 BOX; Type 0: Not a Combination Product03/30/2020
2NDC:80234-9009-350 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
3NDC:80234-9009-4250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/30/2020
4NDC:80234-9009-5500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/30/2020
5NDC:80234-9009-61000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/30/2020
6NDC:80234-9009-73780 mL in 1 BOTTLE, PUMP; 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 - Tavos Industries Inc. (204196534)
Establishment
NameAddressID/FEIBusiness Operations
Tavos Industries Inc.204196534manufacture(80234-9009)

Revised: 2/2022
Document Id: d8a296ab-c10f-082e-e053-2995a90ab2f0
Set id: ada4a381-644f-8c5e-e053-2995a90a7cf3
Version: 2
Effective Time: 20220222
 
Tavos Industries Inc.