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Allure Isopropyl Rubbing Alcohol

Medically reviewed on Jun 29, 2018

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 50mL in 100mL
Labeler: Universal Distribution Center LLC
NDC Code: 52000-001

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.

ALLURE ISOPROPYL RUBBING ALCOHOL

Active Ingredients

Isopropyl alcohol (50% conc.)

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, heat, spark, electrical

Ask a doctor before use if you have
  • deep puncture wounds, animal bites or serious burns

When using this product
  • do not get into eyes
  • do not apply over large areas of body
  • do not use longer than one week unless directed by a doctor

Stop using this product if
  • condition persists or gets worse

Keep this and all drugs out of the reach of childrenIn case of accidental ingestion, seek professional  assistance or contact a Poison control center (1-800-222-1212) immediately

Directions
  • clean affected area
  • apply a small amount of this product on the area 1-3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other information
  • store at room temperature
  • dose not contain, nor is intended as a substitute for grain or  ethyl alcohol
  • will produce serious gastric disturbance if taken internally

Inactive ingredientpurified water

PRINCIPAL DISPLAY PANEL ALLURE ISOPROPYL RUBBING ALCOHOL
FIRST AID ANTISEPTIC
12 FL.OZ (355 mL)



ALLURE ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL50 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
Packaging
#Item CodePackage Description
1NDC:52000-001-01118 mL in 1 BOTTLE, PLASTIC
2NDC:52000-001-02177 mL in 1 BOTTLE, PLASTIC
3NDC:52000-001-03237 mL in 1 BOTTLE, PLASTIC
4NDC:52000-001-04296 mL in 1 BOTTLE, PLASTIC
5NDC:52000-001-05355 mL in 1 BOTTLE, PLASTIC
6NDC:52000-001-06414 mL in 1 BOTTLE, PLASTIC
7NDC:52000-001-07473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333A06/29/2012
Labeler -  Universal Distribution Center LLC (019180459)
Establishment
NameAddressID/FEIOperations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture

 
Universal Distribution Center LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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