Stone Barn Hand Sanitizer

Manufacturer
Stone Barn Brandyworks
Effective date
2020-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:58:13

Label at a glance#

ProductStone Barn Hand Sanitizer
Active ingredientALCOHOL
Label structure14 sections

Dosage and administration

Directions - Place enough product on hands to cover all surfaces. Rub Hands together until dry. - Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredients and Back Label

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient[s]

Alcohol 80% v/v .... Antiseptic

Active Ingredient[s]Active Ingredient[s]

Use[s]

INDICATIONS & USAGE SECTION

Use[s]

Hand Sanitizer to help reduct bacteria that potentially can cause disease. For use when soap and water are not available

Use[s]Use[s]

Warnings

WARNINGS SECTION

Warnings

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

warningswarnings

Do Not Use

OTC - DO NOT USE SECTION

Do not use

- In children less than 2 months of age

- On open skin wounds

Do Not UseDo Not Use

When using this product

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes throughly with water.

When usingWhen using

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

stop usestop use

Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poisen Control Center right away.

Keep out of reachKeep out of reach

Other information

OTHER SAFETY INFORMATION

Other information

- Store between 15-30C (59-86F)

- Avoid freezing and excessive heat aboce 40C (104F)

other informationother information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients glycerin, hydrogen peroxide, purified water USP

Inactive IngredientsInactive Ingredients

Directions

INSTRUCTIONS FOR USE SECTION

Directions

- Place enough product on hands to cover all surfaces. Rub Hands together until dry.

- Supervise children under 6 years of age when using this product to avoid swallowing.

directionsdirections

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

- Place enough product on hands to cover all surfaces. Rub hands together until dry.

- Supervise children under 6 years of age when using this product to avoid swallowing.

directions and dosagedirections and dosage

Warnings

WARNINGS AND PRECAUTIONS SECTION

Warnings

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

warningwarning

Purpose

OTC - PURPOSE SECTION

Use[s]

Hand Sanitizer to help reduce bacteria that potentially cause disease. For use when soap and water are not available.

purposepurpose

Front Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Antiseptic 80% Topical Solution

Hand Sanitizer

Non-sterile Solution

4 fl oz

WHO Formulation #1

Produced by

Stone Barn Brandyworks

Portland, Oregon

front labelfront label

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
73854-000173854-0001-1, 73854-0001-2, 73854-0001-3, 73854-0001-4, 73854-0001-5

Ingredients#

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

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

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
b7cb6df8-1824-09f9-e053-2a95a90acc19a1dc62d1-bc57-7925-e053-2a95a90a405f2020-12-31WarningsExact identifier
spl id: b7cb6df8-1824-09f9-e053-2a95a90acc19
spl set id: a1dc62d1-bc57-7925-e053-2a95a90a405f

Reported adverse events (FAERS/openFDA)#

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