FDA.reportPublic FDA data

HAND SANITIZER 8OZ

Manufacturer
Pocket Nurse Enterprises, Inc.
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:26:13

Label at a glance#

ProductHAND SANITIZER 8OZ
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

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

Dosage and administration

wet hands thoroughly with product 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 105 Fahrenheit may discolor some fabrics harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70 percent

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

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 and flame.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if skin irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product 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 105 Fahrenheit
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77629-13177629-131-01

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
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER 934Z135WT9208IACT
AMINOMETHYL PROPANEDIOLCZ7BU4QZJZIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a7a4eebf-a995-6443-e053-2a95a90aff4ba7a4eebf-a994-6443-e053-2a95a90aff4b2020-06-01WarningsExact identifier
spl id: a7a4eebf-a995-6443-e053-2a95a90aff4b
spl set id: a7a4eebf-a994-6443-e053-2a95a90aff4b

Reported adverse events (FAERS/openFDA)#

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