FDA.reportPublic FDA data

Dial Antimicrobial

Manufacturer
Bocchi Laboratories | Henkel Corporation
Effective date
2021-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:23

Label at a glance#

ProductDial Antimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient



Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose



Antibacterial

INDICATIONS & USAGE SECTION

Uses

  • For handwashing to decrease bacteria on the skin

WARNINGS SECTION

Warnings

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • if irritation or redness develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • Pump into dry hands.
  • Lather vigorously for at least 15 seconds
  • Rinse thouroughly and dry

INACTIVE INGREDIENT SECTION

Aqua (Water, Eau), Glycerin, Lauramine Oxide, Cetrimonium Chloride, Cocamidopropyl Betaine, Sodium Benzoate, Hydroxypropyl Methylcellulose, Parfum (Fragrance), Zinc Sulfate, Sodium Chloride, Dimethyl Lauramine, Tetrasodium EDTA, Alcohol, Dimethyl Myristamine, CI 42090 (Blue 1), CI 17200 (Red 33).

OTC - WHEN USING SECTION

When using this product

Avoid contact with eyes, in case of eye contact, flush with water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DFHWDFHW

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57702-501-082023-01-30C16284748780-1f386c649-fe18-0266-e053-dadaa90a7c1aDial Antimicrobial

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57702-501-08Dial Antimicrobial221 mL in 1 BOTTLE, PUMPLIQUID2211

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57702-501DIAL ANTIMICROBIAL (BENZALKONIUM CHLORIDE) LIQUID [BOCCHI LABORATORIES]1Legacy NDC, 1 package rows20210515_c2192969-7a24-16c6-e053-2a95a90ad979.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57702-50157702-501-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHYL LAURAMINE6V2OM30I1ZIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
GLYCERINPDC6A3C0OXIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
DIMETHYL MYRISTAMINE5E4O85D8T2IACT
SODIUM BENZOATEOJ245FE5EUIACT
ALCOHOL3K9958V90MIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
ZINC SULFATE89DS0H96TBIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
EDETATE SODIUMMP1J8420LUIACT

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
c2192983-842e-510e-e053-2a95a90a2429c2192969-7a24-16c6-e053-2a95a90ad9792021-05-11WarningsExact identifier
spl id: c2192983-842e-510e-e053-2a95a90a2429
spl set id: c2192969-7a24-16c6-e053-2a95a90ad979

Reported adverse events (FAERS/openFDA)#

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