FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Daisy Nail Products, Inc.
Effective date
2020-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:24:19

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hand thoroughly and allow to dry without wiping For children under 6, use only under adult supervision not recommended for infants

Storage and handling

do not store above 105F may discolor some fabrics harmful to wood finish and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

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

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin
  • do not inhale or ingest

OTC - STOP USE SECTION

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

  • Wet hand thoroughly 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

do not store above 105F

may discolor some fabrics

harmful to wood finish and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, butanediol, carboxypolymethylene, viatmine E and aloe vera extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 mL NDC: 78951-001-01

PDPPDP500 mL NDC: 78951-001-02

PDPPDP

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78951-00178951-001-01, 78951-001-02
76925-001

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
1,2-BUTANEDIOLRUN0H01QEUIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOXYPOLYMETHYLENE0A5MM307FCIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT

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
c48a7772-f771-797b-e053-2a95a90a909fa825b8c5-1ac3-6c82-e053-2995a90ad5232021-06-11WarningsExact identifier
spl set id: a825b8c5-1ac3-6c82-e053-2995a90ad523

Reported adverse events (FAERS/openFDA)#

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