FDA.reportPublic FDA data

DawnMist Antiperspirant

Manufacturer
Dukal LLC
Effective date
2025-01-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:50:31

Label at a glance#

ProductDawnMist Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 4.5%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use on broken skin

Ask a doctor before use

OTC - STOP USE SECTION

Ask a doctor before use if you have kidney disease.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If accidently swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butylated Hydroxytoluene, Cetylstearyl Alcohol, Diazolidinyl Urea, Dimethicone, Disodium EDTA, Glycerin, Glyceryl stearate, Hydroxyethylcellulose, Methylparaben, Mineral Oil, Propylparaben, Sorbitan Monostearate, Stearic acid, Triethylamine, Tween-60, Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DawnMist

Roll-On

Antiperspirant

Fragrance Free

NDC 65517-2032-1

Dukal

2FL.OZ. (59ml)

RD20RD20

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65517-2032-1DawnMist Antiperspirant59 mL in 1 BOTTLELOTION592

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65517-2032DAWNMIST ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LOTION [DUKAL LLC]2Current NDC, 1 package rows20250104_1fbdd228-e26a-275b-e063-6394a90a4c2f.zip

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
65517-203265517-2032-1

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
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
SORBITAN MONOSTEARATENVZ4I0H58XIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
MINERAL OILT5L8T28FGPIACT
EDETATE DISODIUM7FLD91C86KIACT
POLYSORBATE 60CAL22UVI4MIACT
GLYCERINPDC6A3C0OXIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
WATER059QF0KO0RIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
TRIETHYLAMINEVOU728O6AYIACT
STEARIC ACID4ELV7Z65APIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
DIMETHICONE92RU3N3Y1OIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT

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
DawnMist AntiperspirantALUMINUM CHLOROHYDRATEDukal LLC1fbdd228-e26a-275b-e063-6394a90a4c2f2025-01-02WarningsExact identifier
ndc (package): 65517-2032-1
ndc (product): 65517-2032
ndc11 (package): 65517203201
spl id: 2969b490-0bb9-21fe-e063-6394a90a5f2e
spl set id: 1fbdd228-e26a-275b-e063-6394a90a4c2f

Reported adverse events (FAERS/openFDA)#

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