Daisy DND

Manufacturer: Daisy Nail Product Inc.
Effective date: 2020-06-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:35

Label at a glance#

ProductDaisy DND

Active ingredientALCOHOL

Label structure9 sections

Dosage and administration

Spray on to hands and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Storage and handling

Store between 20°C-25°C (68-77°F). May discolor certain fabrics and surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only- hands.
Flammable, keep away from heat or flame.
Do not use

in children less than 2 months of age
on open skin wounds

When using this product

keep out of eyes, in case of contact with eyes, rinse eyes thoroughly with water.
avoid contact with broken skin.
do not inhale or ingest.

Stop use and ask a doctor if skin irritation 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray on to hands and allow to dry without wiping.
For children under 6, use only under adult supervision.
Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

Store between 20°C-25°C (68-77°F).
May discolor certain fabrics and surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Jojoba oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 80 mL

Label 100 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286295	ethanol 75 % Topical Spray	PSN	1
2286295	ethanol 0.75 ML/ML Topical Spray	SCD	1
2286295	ethanol 75 % Topical Spray	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78951-004-01	2022-01-28	C162847	48780-1	d6a99b39-750b-a426-e053-dadaa90af4c2	5bbe7f3a-6617-40c2-acff-932214b957c7
78951-004-02	2022-01-28	C162847	48780-1	d6a99b39-750b-a426-e053-dadaa90af4c2	5bbe7f3a-6617-40c2-acff-932214b957c7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78951-004-01	Daisy DND	80 mL in 1 BOTTLE, PLASTIC	SPRAY	80		1
78951-004-02	Daisy DND	240 mL in 1 BOTTLE, PLASTIC	SPRAY	240		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78951-004	DAISY DND (ALCOHOL) SPRAY [DAISY NAIL PRODUCT INC.]	1	Legacy NDC, 2 package rows	20200614_5bbe7f3a-6617-40c2-acff-932214b957c7.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Daisy DND
Alcohol
JOJOBA OIL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78951-004	78951-004-01, 78951-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
JOJOBA OIL	724GKU717M	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
092314b6-252a-4dab-b9c7-aa5b6ad4dd3a			5bbe7f3a-6617-40c2-acff-932214b957c7	2020-06-10	Warnings	Exact identifier spl id: 092314b6-252a-4dab-b9c7-aa5b6ad4dd3a spl set id: 5bbe7f3a-6617-40c2-acff-932214b957c7

Reported adverse events (FAERS/openFDA)#

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