ETHYL RUBBING ALCOHOL- ethyl rubbing alcohol liquid 
P & L Development, LLC

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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Drug Facts

Active Ingredients

Ethyl Alcohol (70 percent concentration)

Purpose

first aid antiseptic

Uses

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

Ask a doctor before use if you have

deep or puncture wounds, animal bites or serious burns

When using this product

do not get into eyes

do not apply over large areas of the body

do not use longer than one week unless directed by a doctor

Stop use and ask a doctor if

conditions persists or gets worse

Keep this and all drugs out of the reach of children

In case of accidental ingestion seek professional assistance, or contact a poison control center immediately

Directions

clean affected area

apply small amount of this product on the area 1-3 times daily

may be covered with a small bandage

If bandaged, let dry first

Other Information

store at controlled room temperature

will produce serious gastric disturbances if taken internally

Inactive Ingredient

acetone, denatonium benzoate, methyl isobutyl ketone, purified water

principal display panel

Aaron Brands

Ethyl

Rubbing Alcohol

70% by Volume

16 FL OZ (1 PT.) 473 mL

image of label


ETHYL RUBBING ALCOHOL 
ethyl rubbing alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49580-0905
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)  
ACETONE (UNII: 1364PS73AF)  
METHYL ISOBUTYL KETONE (UNII: U5T7B88CNP)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49580-0905-1473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/03/200912/31/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A10/03/200912/31/2019
Labeler - P & L Development, LLC (101896231)

Revised: 4/2019
 
P & L Development, LLC