FDA.reportPublic FDA data

Arizona Biltmore Hand Sanitizer

Manufacturer
A.D.S. Sales Co. Inc.
Effective date
2021-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:24:53

Label at a glance#

ProductArizona Biltmore Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

To help reduce bacteria on the skin.

Dosage and administration

Squeeze a significant amount in your palm and rub hands until fully dry. Rinse free.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 72% (v/v)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable.
  • Keep away from fire or flame. 

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop using and ask a doctor if

OTC - STOP USE SECTION

  • Irritation or redness develops and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • In case of accidental ingestion, get medical help or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Squeeze a significant amount in your palm and rub hands until fully dry.
  • Rinse free.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Hydrolyzed Jojoba Esters, Phenoxyethanol, Parfum(Fragrance), Aminomethyl Propanol, Tocopherol, Glycine Soja (Soybean) Oil, Aloe Barbadensis Leaf Juice, Citrus Aurantium Dulcis (Orange) Fruit Extract, Olea Europaea (Olive) Fruit Oil

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 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79249-02879249-028-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
PHENOXYETHANOLHIE492ZZ3TIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
TOCOPHEROLR0ZB2556P8IACT
SOYBEAN OIL241ATL177AIACT
ALOE VERA LEAFZY81Z83H0XIACT
ORANGE5EVU04N5QUIACT
OLIVE OIL6UYK2W1W1EIACT
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
f7ab9ac6-fcb2-3dd4-e053-6394a90a6e4cb62029af-3a78-cc79-e053-2a95a90a70482023-03-24WarningsExact identifier
spl set id: b62029af-3a78-cc79-e053-2a95a90a7048

Reported adverse events (FAERS/openFDA)#

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