FDA.reportPublic FDA data

DawnMist Antibacterial

Manufacturer
Dukal LLC
Effective date
2023-10-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:24:14

Label at a glance#

ProductDawnMist Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes. If contact occurs, rinse eyes with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develops
  • condition persists for more than 72 hours

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

  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, cetrimonium chloride, decyl glucoside, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 33, red 40, yellow 5

Principal Display Panel - DawnMist Handwashing Antibacterial Hand Soap Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel - DawnMist Handwashing Antibacterial Hand Soap LabelPrincipal Display Panel - DawnMist Handwashing Antibacterial Hand Soap LabelDawnMist®

HANDWASHING

Antibacterial



Hand Soap

LIGHT FRESH SCENT



pH BALANCED

DERMATOLOGIST TESTED

8 FL OZ (236 mL)

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65517-102265517-1022-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-150 DISTEARATE6F36Q0I0ACIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
DISTEARETH-75 ISOPHORONE DIISOCYANATE5365FJ30SCIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
SODIUM CHLORIDE451W47IQ8XIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
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
07d56ed4-466b-dd20-e063-6394a90aa6863abfd7f5-a7ea-4e7a-80c4-ba3fcb4cc6e32023-10-16WarningsExact identifier
spl set id: 3abfd7f5-a7ea-4e7a-80c4-ba3fcb4cc6e3

Reported adverse events (FAERS/openFDA)#

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