FDA.reportPublic FDA data

DawnMist Antiperspirant Spray 4.5%

Manufacturer
Dukal LLC
Effective date
2024-12-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:45:19

Label at a glance#

ProductDawnMist Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 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.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

Do not use on broken skin

Stop use

OTC - STOP USE SECTION

Stop use if rash or irritation occurs.

Ask a doctor before use

OTC - ASK DOCTOR 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

Alcohol, Fragrance, PEG-40 Hydrogenated Castor Oil, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DawnMist

Antiperspirant

Spray

Fresh Scent

NDC 65517-2030-1

Dukal

2FL.OZ. (59ml)

PSD20PSD20

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 65517-2030-2

DawnMist

Personal Care

Antiperspirant

Spray

Fresh Scent

4FL.OZ. (118ml)

PSD40PSD40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65517-2030-1DawnMist Antiperspirant59 mL in 1 BOTTLE, SPRAYLIQUID592
65517-2030-2DawnMist Antiperspirant118 mL in 1 BOTTLE, SPRAYLIQUID1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65517-2030DAWNMIST ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) LIQUID [DUKAL LLC]2Current NDC, 2 package rows20241222_1e01ecd8-8271-3947-e063-6294a90a69c6.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65517-203065517-2030-1, 65517-2030-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
WATER059QF0KO0RIACT
ALCOHOL 95%7528N5H79BIACT

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 LLC1e01ecd8-8271-3947-e063-6294a90a69c62024-12-19WarningsExact identifier
ndc (package): 65517-2030-1
ndc (package): 65517-2030-2
ndc (product): 65517-2030
ndc11 (package): 65517203001
ndc11 (package): 65517203002
spl id: 29a7e1ed-c883-438b-e063-6394a90a0cb4
spl set id: 1e01ecd8-8271-3947-e063-6294a90a69c6

Reported adverse events (FAERS/openFDA)#

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