REXALL ALCOHOL PREP- isopropyl alcohol swab 
Dolgencorp, 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.

----------

55910-809 Dolgencorp Rexall IPA pads

Active ingredient

Isopropyl alcohol 70% w/w

Purpose

Antiseptic

Uses

  • • 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

  • • with electrocautery procedures
  • • longer than 1 week unless directed by a doctor

When using this product

  • • do not get into eyes
  • • do not apply over large areas of the body
  • • in case of deep or puncture wounds, animal bites or serious berns, consult a doctor

Stop use and ask a doctor if

  • • irritation and redness develop
  • • condition gets worse or persists for more than 72 hours

Keep out of reach of children.

If accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • • apply to skin as needed
  • • discard after single use

Other information

  • • protect from freezing and avoid excessive heat
  • • not made with natural rubber latex

Inactive ingredients

water

Manufacturing Information

Distributed by:

Dolgencorp, LLC

100 Mission Ridge, Goodlettsville, TN 37072 USA

Packaged in China with components from Taiwan

1-866-4-REXALL

www.Rexall.com

REF: DG090737RCV1

V1 RI19LPD

Package Label

Label

REXALL ALCOHOL PREP 
isopropyl alcohol swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-809
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:55910-809-30100 in 1 BOX07/01/201009/30/2023
1NDC:55910-809-091 in 1 PACKET
15 mL in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A07/01/201009/30/2023
Labeler - Dolgencorp, LLC (068331990)
Registrant - Medline Industries, LP (025460908)

Revised: 8/2023
Document Id: 037086ea-57be-ae42-e063-6294a90a2657
Set id: e6a72646-f0f8-4184-8625-8b36e55d1c59
Version: 5
Effective Time: 20230821
 
Dolgencorp, LLC