FDA.reportPublic FDA data

Antibacterial Body Wash

Manufacturer
Vi-Jon
Effective date
2020-07-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:20:10

Label at a glance#

ProductAntibacterial Body Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

work a small amount into a lather scrub thoroughly rinse

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

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

  • work a small amount into a lather
  • scrub thoroughly
  • rinse

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, PEG-120 methyl glucose dioleate, cetrimonium chloride, glycerin, lauramidopropylamine oxide, cocamide MEA, fragrance, sodium sulfate, myristamidopropylamine oxide, sodioum chloride, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antibacterial Body Wash

21 FL OZ (621 mL)

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11344-337-562024-12-18C16284748780-19d75b9d0-af1b-f424-e053-dadaa90a57ce344e81e4-6d0c-4049-bf9d-a96039028003
11344-337-562022-01-28C16284748780-19d75b9d0-af1b-f424-e053-dadaa90a57ce344e81e4-6d0c-4049-bf9d-a96039028003
11344-337-562020-07-27C16284748780-19d75b9d0-af1b-f424-e053-dadaa90a57ce344e81e4-6d0c-4049-bf9d-a96039028003
11344-337-562020-01-31C16284748780-19d75b9d0-af1b-f424-e053-dadaa90a57ce344e81e4-6d0c-4049-bf9d-a96039028003

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11344-33711344-337-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
water059QF0KO0RIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
cetrimonium chlorideUC9PE95IBPIACT
GLYCERINPDC6A3C0OXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
COCO MONOETHANOLAMIDEC80684146DIACT
SODIUM SULFATE0YPR65R21JIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
methylchloroisothiazolinoneDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT

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
29918e42-44d4-1279-e063-6294a90a9eda344e81e4-6d0c-4049-bf9d-a960390280032024-12-18WarningsExact identifier
spl set id: 344e81e4-6d0c-4049-bf9d-a96039028003

Reported adverse events (FAERS/openFDA)#

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