ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol solution 
NDC, Inc.

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Isopropyl Rubbing Alcohol

Drug Facts

Active Ingredient

Isopropyl Alcohol 70% v/v

Purpose

First Aid Antiseptic

Uses

First aid to help prevent the risk of infection in:

WARNINGS

For external use only

Flammable

  • keep away from fire or flame, heat, spark, electrical. Flash point 72°F
  • do not use with electrocautery procedures.

Ask a doctor before use if you havedeep 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 1 week unless directed by a doctor

Stop use and ask a doctor if

  • the condition persists or gets worse

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive Ingredient

Purified Water

PRINCIPAL DISPLAY PANEL 

REF: P907132

NDC 43128-002-32

Pro
ADVANTAGE®

Isopropyl Rubbing
Alcohol 70% USP

Tamper evident cap for your protection.
If ring-band is detached from cap or missing do not use.

WARNING:Flammable

Made in USA for:
NDC, Inc., 407 New Sanford Rd.
La Vergne, TN 37086
www.ProAdvantagebyNDC.com

32 fl. oz. (946 mL)

PRINCIPAL DISPLAY PANEL

ISOPROPYL RUBBING ALCOHOL 
isopropyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43128-002-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
2NDC:43128-002-013785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
3NDC:43128-002-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00306/01/2014
Labeler - NDC, Inc. (009831413)

Revised: 10/2023
Document Id: 08b8bdab-eaad-bc6b-e063-6394a90a0f3e
Set id: 07bfadf4-7452-4c7a-b60e-feb658b92e73
Version: 8
Effective Time: 20231027
 
NDC, Inc.