DawnMist Alcohol Hand Sanitizer

Manufacturer: Dukal LLC
Effective date: 2023-10-13
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:56:46

Label at a glance#

ProductDawnMist Alcohol Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

wet hands thoroughly with products and allow to dry without wiping. for children under 6, use only under adult supervision

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Warning

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes, ears and mouth. In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with products and allow to dry without wiping.

for children under 6, use only under adult supervision

Other Information

OTHER SAFETY INFORMATION

Avoid freezing and excessive heat above 104°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-30Alkyl Acrylate Cross Polymer, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Triethanolamine, Water

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HS8004NDC 65517-1023-1

DawnMist ®

Hand Sanitizer

Drug Facts

Active Ingredient Purpose

Ethyl alcohol 62%.........Antiseptic

REF HS8004

4 FL. OZ. (118 ml)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	4
581660	ethanol 0.62 ML/ML Topical Gel	SCD	4
581660	ethanol 62 % Topical Gel	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65517-1023-1	DawnMist Alcohol Hand Sanitizer	118 mL in 1 BOTTLE	GEL	118		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65517-1023	DAWNMIST ALCOHOL HAND SANITIZER (ALCOHOL) GEL [DUKAL LLC]	4	Current NDC, Legacy NDC, 1 package rows	20231014_a2df96a9-8514-6839-e053-2a95a90a9417.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

DawnMist Alcohol Hand Sanitizer
Alcohol
TROLAMINE
WATER
CARBOMER INTERPOLYMER TYPE A (55000 CPS)
MALTODEXTRIN
ALOE VERA LEAF
GLYCERIN
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65517-1023	65517-1023-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
TROLAMINE	9O3K93S3TK	IACT
WATER	059QF0KO0R	IACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)	59TL3WG5CO	IACT
ALCOHOL	3K9958V90M	ACTIB
MALTODEXTRIN	7CVR7L4A2D	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DawnMist Alcohol Hand Sanitizer	ALCOHOL	Dukal LLC	a2df96a9-8514-6839-e053-2a95a90a9417	2023-10-13	Warnings	Exact identifier ndc (package): 65517-1023-1 ndc (product): 65517-1023 ndc11 (package): 65517102301 spl id: 07a03ddc-9f84-25e3-e063-6294a90adae9 spl set id: a2df96a9-8514-6839-e053-2a95a90a9417

Reported adverse events (FAERS/openFDA)#

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