Too People Antiseptic Liquid Hand Sanitizer 80% Ehtyl Alcohol Refill

Too People Antiseptic Liquid Hand Sanitizer 80 Ehtyl Alcohol Refill by

Drug Labeling and Warnings

Too People Antiseptic Liquid Hand Sanitizer 80 Ehtyl Alcohol Refill by is a Otc medication manufactured, distributed, or labeled by Pan American Properties, Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

TOO PEOPLE ANTISEPTIC LIQUID HAND SANITIZER 80 EHTYL ALCOHOL REFILL- alcohol liquid 
Pan American Properties, Corp.

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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Too People Antiseptic Liquid Hand Sanitizer 80% Ehtyl Alcohol Refill

Drug Facts

Active ingredient[s]

Ethyl alcohol 80% v/v

Purpose

Antiseptic

Use[s]

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

Warnings

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

Do not use

• in children less than 2 months of age
• on open skin wounds

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 sign of a serious condition.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, water

Package Labeling: 208.2 l

Package Labeling: 18.9 l

Package Labeling: 3.78 l

Package Labeling: 946 ml

TOO PEOPLE ANTISEPTIC LIQUID HAND SANITIZER 80 EHTYL ALCOHOL REFILL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79368-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79368-001-01	208200 mL in 1 DRUM; Type 0: Not a Combination Product	06/15/2021	06/15/2021
2	NDC: 79368-001-02	18900 mL in 1 PAIL; Type 0: Not a Combination Product	06/15/2021	06/15/2021
3	NDC: 79368-001-03	3780 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2021	06/15/2021
4	NDC: 79368-001-04	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/15/2021	06/15/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	06/15/2021	06/15/2021

Labeler - Pan American Properties, Corp. (167444467)

Revised: 4/2022

Document Id: dda63043-b79f-07ea-e053-2995a90a4d72

34390-5

Set id: c4f8ab80-6690-8a4d-e053-2a95a90ac3a2

Version: 2

Effective Time: 20220427