FDA.reportPublic FDA data

DND hand sanitizer 3.78L

Manufacturer
Daisy Nail Products, Inc.
Effective date
2020-07-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:51

Label at a glance#

ProductDND hand sanitizer 3.78L
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Hand sanitizer to reduce bacteria on the skin that could cause disease. recommended for repeated use

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using

Storage and handling

Do not store above 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antimicrobial

Purpose

OTC - PURPOSE SECTION

Antimicrobial, Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to reduce bacteria on the skin that could cause disease.
  • recommended for repeated use

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame. For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact with eyes, flush eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

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

  1. Place enough product in your palm to thoroughly cover your hands
  2. Rub hands together briskly until dry
  3. Children under 6 years of age should be supervised when using

Other information

STORAGE AND HANDLING SECTION

Do not store above 110F (43C)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), caprylyl glycol, phenoxyethanol, acrylates/c10-30 alkyl acrylate crosspolymer, isopropyl myristate, triethanolamine

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.78L NDC: 78951-005-01

PDPPDP

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78951-00578951-005-01
76925-002

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLYL GLYCOL00YIU5438UIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PHENOXYETHANOLHIE492ZZ3TIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

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
c48a7021-e174-50bb-e053-2a95a90a7de3aa39fd62-d24c-7f21-e053-2a95a90a6da72021-06-11WarningsExact identifier
spl set id: aa39fd62-d24c-7f21-e053-2a95a90a6da7

Reported adverse events (FAERS/openFDA)#

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