READYBATH LUXE- benzalkonium chloride cloth 
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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180 Readybath LUXE (scented)

Active ingredient

Benzalkonium chloride 0.12%

Purpose

Antiseptic

Uses

Warnings

For external use only

Do not use

  • in the eyes

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

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

Keep out of reach of children.

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

Directions

diagram

Other information

Inactive ingredients

water (aqua), cocamidopropyl PG-dimonium chloride phosphate, glycerin, phenoxyethanol, benzoic acid, dehydroacetic acid, ethylhexylglycerin, disodium EDTA, polysorbate 20, sodium citrate, fragrance, simethicone, aloe barbadensis leaf juice

Manufacturing Information

Manufactured by:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with domestic and foreign materials

www.medline.com

1-800-MEDLINE (633-5463)

REF: MSC095100

V1 RK21DYN

Package Label

PDP

READYBATH LUXE 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-180
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.12 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-180-76129 g in 1 PACKAGE; Type 0: Not a Combination Product05/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/2016
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 3/2022
Document Id: da3130f3-a315-b8a3-e053-2995a90a8084
Set id: 32bc07dc-7a9c-63ed-e054-00144ff8d46c
Version: 3
Effective Time: 20220314
 
Medline Industries, LP