FDA.reportPublic FDA data

ReadyBath Select

Manufacturer
Medline Industries, LP
Effective date
2025-06-11
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:02:51

Label at a glance#

ProductReadyBath Select
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

for body cleansing to decrease bacteria on the skin helps kill germs that can cause odor

Dosage and administration

gently pull label tab until package opening is exposed remove cloths one at a time to cleanse body parts in the order of the diagram allow skin to dry dispose of cloth in waste receptacle do not flush cloths in toilet

Storage and handling

avoid excessive heat, protect from freezing washcloth: rayon/polyester

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • for body cleansing to decrease bacteria on the skin
  • helps kill germs that can cause odor

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in the eyes

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • gently pull label tab until package opening is exposed
  • remove cloths one at a time to cleanse body parts in the order of the diagram
  • allow skin to dry
  • dispose of cloth in waste receptacle
  • do not flush cloths in toilet

diagramdiagram

Other information

STORAGE AND HANDLING SECTION

  • avoid excessive heat, protect from freezing
  • washcloth: rayon/polyester

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

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: MSC095105

V1 RH22MSC

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label V1 RH22MSCLabel V1 RH22MSC

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038741benzalkonium Cl 0.12 % Medicated PadPSN7
1038746ReadyBath 0.12 % Medicated PadPSN7
1038746benzalkonium chloride 1.2 MG/ML Medicated Pad [ReadyBath]SBD7
1038741benzalkonium chloride 1.2 MG/ML Medicated PadSCD7
1038741benzalkonium chloride 0.12 % Medicated WipeSY7
1038741benzalkonium chloride 0.12 % Topical ClothSY7
1038741benzalkonium chloride 0.12 % Topical SwabSY7
1038746ReadyBath 0.12 % Medicated PadSY7
1038746ReadyBath 1.2 MG/ML Medicated PadSY7

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53329-183-76ReadyBath Select91 g in 1 PACKAGECLOTH917

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53329-18353329-183-76

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
DEHYDROACETIC ACID2KAG279R6RIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
BENZOIC ACID8SKN0B0MIMIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
DIMETHICONE92RU3N3Y1OIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM CITRATE1Q73Q2JULRIACT
EDETATE DISODIUM7FLD91C86KIACT
POLYSORBATE 207T1F30V5YHIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ReadyBath SelectBENZALKONIUM CHLORIDEMedline Industries, LP3338023a-171e-1e49-e054-00144ff8d46c2025-06-11WarningsExact identifier
ndc (package): 53329-183-76
ndc (product): 53329-183
ndc11 (package): 53329018376
spl id: 374dfd20-a0e5-70ba-e063-6294a90a5667
spl set id: 3338023a-171e-1e49-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.