MEDLINE- benzalkonium chloride, lidocain hydrochloride spray 
Medline Industries, LP

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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918 Medline Cleansing Spray

Active ingredients

Benzalkonium chloride 0.13% w/w

Lidocaine HCl 4% w/w

Purpose

First aid antiseptic, Topical pain reliever

Uses

Warnings

For external use only.

Do not use

  • in the eyes or apply over large areas of the body
  • longer than 1 week, unless directed by a doctor
  • in large quantities, particularly over raw surfaces or blistered areas

Ask a doctor before use if you have

  • deep puncture wounds, animal bites, or serious burns

When using this product

  • contents under pressure
  • do not puncture or incinerate
  • store at temperatures between 45°-130°F (7°-54°C), avoid excessive heat

Stop use and consult a doctor if

  • condition persists or gets worse

Keep out of reach of children.

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

Directions

Inactive ingredients

camphor, propylene glycol, purified water, sodium hydroxide

Questions or comments?

1-800-MEDLINE Monday-Friday 8:30 a.m.-5:00 p.m. EST

Manufacturing Information

Manufactured for: Medline Industries, Inc.

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA of foreign and domestic materials

www.medline.com

1-800-MEDLINE

REF: MDSCLEAN4

V1RF21WIP

Package Label

Package Label

MEDLINE 
benzalkonium chloride, lidocain hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-918
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-918-04113 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/2021
Labeler - Medline Industries, LP (025460908)

Revised: 7/2022
Document Id: e4bb242e-4ddc-632d-e053-2995a90ad20c
Set id: b1059e68-b240-056c-e053-2995a90a61b2
Version: 4
Effective Time: 20220726
 
Medline Industries, LP