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Isopropyl Rubbing Alcohol 70 by Delon Laboratories (1990) Ltd.

Medically reviewed on November 3, 2017

Dosage form: solution
Ingredients: ISOPROPYL ALCOHOL 70mL in 100mL
Labeler: Delon Laboratories (1990) Ltd.
NDC Code: 61734-012

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.

Drug Facts

Active Ingredient (by volume)

Isopropyl alcohol 70%

Purpose

First-aid antiseptic

Uses

First aid to help decrease the risk of infections in minor cuts, scrapes and burns.

Directions
  • clean the affected area
  • apply a small amount of product on the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first
  • for rubbing, apply liberally and rub with hands

Inactive Ingredient

‚ÄčPurified Water

Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Centre immediately.

Warnings

For external use only

  • flammable, keep away from fire or flame
  • will produce serious gastric disurbances if taken internally

Ask a physician before use if you have

  • deep or puncture wounds, animal bites or serious burns

When using this product

  • do not get into eyes or mucous membranes
  • do not apply over large areas of the body
  • do not use longer than one week unless directed by a doctor
  • use only in well ventilated area

Stop use and ask physician if

  • the condition persists or gets worse

Other Information
  • store at room temperature
  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

apply a small amount of product on the area 1 to 3 times daily

ISOPROPYL RUBBING ALCOHOL 70 
isopropyl alcohol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61734-012
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER30 mL  in 100 mL
Packaging
#Item CodePackage Description
1NDC:61734-012-01473 mL in 1 BOTTLE, PLASTIC
2NDC:61734-012-02118 mL in 1 BOTTLE, PLASTIC
3NDC:61734-012-03250 mL in 1 BOTTLE, PLASTIC
4NDC:61734-012-041000 mL in 1 BOTTLE, PLASTIC
5NDC:61734-012-053780 mL in 1 BOTTLE, PLASTIC
6NDC:61734-012-06100 mL in 1 BOTTLE, SPRAY
7NDC:61734-012-07355 mL in 1 BOTTLE, PLASTIC
8NDC:61734-012-08946 mL in 1 BOTTLE, PLASTIC
9NDC:61734-012-09174 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/07/2010
Labeler - Delon Laboratories (1990) Ltd. (248364184)
Establishment
NameAddressID/FEIOperations
Delon Laboratories (1990) Ltd243387722label(61734-012), manufacture(61734-012), pack(61734-012)

 
Delon Laboratories (1990) Ltd.

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Further information

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

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