Too people Denatured 70 % ethyl alcohol

Too people Denatured 70 ethyl alcohol by

Drug Labeling and Warnings

Too people Denatured 70 ethyl alcohol 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 DENATURED 70 ETHYL ALCOHOL- 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 Denatured 70 % ethyl alcohol

Drug Facts

Active ingredient[s]

Ethyl alcohol 70% v/v

Purpose

Antibacterial Agent

Use[s]

Cleans skin and kills bacteria.

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 wih 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 at 1-800-222-1222.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Superivse 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

water

Package Labeling:

Label2

TOO PEOPLE DENATURED 70 ETHYL ALCOHOL 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79368-006
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
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79368-006-013780 mL in 1 BOTTLE; Type 0: Not a Combination Product05/04/202003/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/04/202003/30/2022
Labeler - Pan American Properties, Corp. (167444467)

Revised: 4/2022
Document Id: dda67851-691e-153c-e053-2995a90a135a
Set id: c4e83743-788c-43ae-85b3-fe528c5c19a5
Version: 2
Effective Time: 20220427