ALLURE ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol liquid

Allure Isopropyl Rubbing Alcohol by

Drug Labeling and Warnings

Allure Isopropyl Rubbing Alcohol by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC, Anicare Pharmaceuticals Pvt. Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 children

In 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 ingredient

purified water

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

ALLURE ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	50 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-001-01	118 mL in 1 BOTTLE, PLASTIC
2	NDC: 52000-001-02	177 mL in 1 BOTTLE, PLASTIC
3	NDC: 52000-001-03	237 mL in 1 BOTTLE, PLASTIC
4	NDC: 52000-001-04	296 mL in 1 BOTTLE, PLASTIC
5	NDC: 52000-001-05	355 mL in 1 BOTTLE, PLASTIC
6	NDC: 52000-001-06	414 mL in 1 BOTTLE, PLASTIC
7	NDC: 52000-001-07	473 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333A	06/29/2012

Labeler -  Universal Distribution Center LLC (019180459)

Establishment
Name	Address	ID/FEI	Business Operations
Anicare Pharmaceuticals Pvt. Ltd		916837425	manufacture