FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Pan American Properties, Corp.
Effective date
2020-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:22:38

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

To decrease disease causing bacteria on skin. For proper use do not dilute. Recomended for repeated use.

Dosage and administration

Apply enough to wet hands, rub until dry. Not recomended for infants. Children under 6 use under adult supervision.

Label contents#

Full prescribing information#

Medicinal Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Non - Medicinal:

INACTIVE INGREDIENT SECTION

Water, Coconut Oil, Orange Oil.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply enough to wet hands, rub until dry.
  • Not recomended for infants.
  • Children under 6 use under adult supervision.

Uses

INDICATIONS & USAGE SECTION

  • To decrease disease causing bacteria on skin.
  • For proper use do not dilute.
  • Recomended for repeated use.

WARNING

WARNINGS SECTION

Flamable, keep away from flame and heat. For external use only (hands).

Keep out of reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek profesional help or contact a Poison Control Center immediately. Discontinue use if skin becomes irritated and consult a physician.

When using this product:

OTC - WHEN USING SECTION

Avoid contact with broken skin. Do not inhale or ingest. Keep out of eyes, in case of contact with eyes flush thoroughly with water.

SPL UNCLASSIFIED SECTION

Do not store above 105° F. Damaging for wood finishes and plastics. May discolor some fabrics.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79368-00079368-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCONUT OILQ9L0O73W7LIACT
ORANGE OILAKN3KSD11BIACT
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
dda66a89-0ed1-1540-e053-2995a90a8285aa072f84-31b4-9f36-e053-2a95a90a3ba02022-04-27WarningsExact identifier
spl set id: aa072f84-31b4-9f36-e053-2a95a90a3ba0

Reported adverse events (FAERS/openFDA)#

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