ISOPROPYL RUBBING ALCOHOL 99%- isopropyl alcohol liquid 
Universal Distribution Center 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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Isopropyl Rubbing Alcohol 99%

Drug Facts

Active Ingredients (by volume):

Isopropyl alcohol (99% conc.)

Purpose

First aid antiseptic

Uses

Warnings

For external use only; flammable, keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

deep punctured 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 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

Other information

Inactive Ingredient Purified Water

FIRST AID ANTISEPTIC

For Rubbing & Massaging

Use only in a well ventilated area:

Fumes may be harmful.

WARNING FLAMMABLE!

Keep away from fire or flame!

TAMPER EVIDENT: DO NOT USE IF THE UNDER CAP SAFETY FOIL IS BROKEN OR MISSING.

Made in India

Distributed by: Universal Distribution Center

96 Distribution Boulevard • Edison, NJ 08817

Packaging

label

ISOPROPYL RUBBING ALCOHOL 99% 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52000-030
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL99 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52000-030-01118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
2NDC:52000-030-02177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
3NDC:52000-030-03237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
4NDC:52000-030-04296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
5NDC:52000-030-05355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
6NDC:52000-030-06414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
7NDC:52000-030-07473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/04/2016
Labeler - Universal Distribution Center LLC (019180459)
Registrant - Anicare Pharmaceuticals Pvt. Ltd (916837425)
Establishment
NameAddressID/FEIBusiness Operations
Anicare Pharmaceuticals Pvt. Ltd916837425manufacture(52000-030)
Establishment
NameAddressID/FEIBusiness Operations
NOWREZ & ISMAIL SHUKRI COMPANY534665497manufacture(52000-030)

Revised: 10/2020
Document Id: bd776b08-984d-4132-b7f0-87807d84fd0e
Set id: a6d082ac-47b1-4847-b075-630892071885
Version: 2
Effective Time: 20201007
 
Universal Distribution Center LLC