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Rexall Alcohol Prep

Dosage form: swab
Ingredients: ISOPROPYL ALCOHOL 70mL in 100mL
Labeler: Dolgencorp, LLC
NDC Code: 55910-809

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

Isopropyl alcohol, 70% w/w

Purpose

Antiseptic

Uses
  • for preparation of the skin prior to injection
  • first aid to help reduce infection in minor cuts, scrapes and burns

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

deep cuts 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 with electrocautery procedures
  • use only in well-ventilated area, fumes may be toxic.

Stop use and ask a doctor if

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

Preparation of the skin prior to injection: wipe injection site vigorously.

First aid antiseptic:

  • Clean the affected area.
  • Wipe the affected area 1 to 3 times daily.
  • May be covered with a sterile bandage.
  • If bandaged, let dry first.

Other information
  • protect from freezing
  • avoid excessive heat

Inactive ingredients

water

Package/Label Principal Display Panel

Rexall Alcohol Prep Pads

Rexall

Antiseptic

Alcohol Prep Pads

Isopropyl alcohol 70%

2-Ply Pads

INDIVIDUALLY WRAPPED

LATEX FREE

100 PADS

Package/Label Back

Rexall Alcohol Prep Pads

REXALL ALCOHOL PREP 
isopropyl alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-809
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
WATER 
Packaging
#Item CodePackage Description
1NDC:55910-809-30100 PACKET in 1 BOX
1NDC:55910-809-091 APPLICATOR in 1 PACKET
15 mL in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/01/2010
Labeler - Dolgencorp, LLC (068331990)

Revised: 12/2012
Document Id: 91f48dbc-954a-4462-a7be-c898a43a9abb
Set id: e6a72646-f0f8-4184-8625-8b36e55d1c59
Version: 2
Effective Time: 20121207
 
Dolgencorp, LLC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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