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

Denatured ethyl alcohol 70%

Purpose

Antiseptic

Use

First aid to help prevent the risk of infection in minor cuts, scrapes and burns.

Warnings

For external use only

Flammable, keep away from fire or flame

Do not use

in the eyes

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Clean affected area. Apply 1 to 3 times daily.

Other information

  • Do not store above 105°F
  • Damaging for wood finishes and plastics
  • May discolor some fabric

Inactive ingredients

Orange oil, water

Package Labeling: 18.9 L

Label

Package Labeling: 208.2 L

Label2

Package Labeling: 946 mL

Label3

TOO PEOPLE DENATURED 70 ETHYL ALCOHOL 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79368-003
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
ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79368-003-0118900 mL in 1 PAIL; Type 0: Not a Combination Product05/04/202003/31/2022
2NDC: 79368-003-02208200 mL in 1 DRUM; Type 0: Not a Combination Product05/04/202003/31/2022
3NDC: 79368-003-03946 mL in 1 BOTTLE; Type 0: Not a Combination Product05/04/202003/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E05/04/202003/31/2022
Labeler - Pan American Properties, Corp. (167444467)

Revised: 4/2022
Document Id: dda5c82f-29f1-5c2b-e053-2995a90ad77c
Set id: cd134645-8ff1-c941-e053-2a95a90af7fe
Version: 2
Effective Time: 20220427