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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919 Medline Burn Spray

Active ingredient

Benzalkonium chloride 0.13% w/w

Lidocaine HCl 4% w/w

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

aloe vera gel, camphor, propylene glycol, purified water USP, 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: MDSBURN4

V1RF21WIP

Purpose

First aid antiseptic

Topical pain reliever

Package Label

Package Label

MEDLINE 
benzalkonium chloride, lidocain hydrochloride spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-919
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-919-04113 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: e4bb1616-5bab-b414-e053-2995a90ae42c
Set id: b0b5ff82-db36-7708-e053-2a95a90ad9bb
Version: 4
Effective Time: 20220726
 
Medline Industries, LP