Symmetry Foaming Hand Sanitizer

Manufacturer
Buckeye International, Inc. | ABC Compounding Co., Inc.
Effective date
2017-12-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:06:32

Label at a glance#

ProductSymmetry Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Use for hand-sanitizing to decrease bacteria on the skin, only when water is not available

WARNINGS SECTION

Warnings

Flammable.

Contents Under Pressure.

Do not puncture or incinerate.

Do not store near fire or flame.

Do not expose to temperatures above 125 F.

Keep away from fire or flames.

For external use only.

OTC - WHEN USING SECTION

When using this product

do not get into eyes

If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation and redness develop

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

DOSAGE & ADMINISTRATION SECTION

Directions

press valve once to deliver one squirt (about a quarter size) of foaming product into the palm of your hand

rub hands together and allow to dry without wiping

INACTIVE INGREDIENT SECTION

Inactive ingredients

water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol, polysorbate 65, dimethicone PEG-8 meadowfoamate, meadowfoamamidopropyl betaine, butane, propane, fragrance

OTC - QUESTIONS SECTION

Questions?

Call: Buckeye International,Inc.314-291-1900

Monday through Friday 8:00 to 5:00 p.m. CST

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

symmetry

AEROSOL

FOAMING HAND

SANITIZER

Symmetry Aerosol Foaming Hand

Sanitizer helps reduce bacteria on the

skin that could cause disease.

Recommended for repeated use.

NET WT. 20 oz (567 grams)

container labelcontainer label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
30805-011-202023-06-13C16284748780-19d75b9d0-6ead-f424-e053-dadaa90a57ceDrug Facts
30805-011-202020-01-31C16284748780-19d75b9d0-6ead-f424-e053-dadaa90a57ceDrug Facts

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
30805-01130805-011-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
31d1cd40-8366-2ea0-e063-6294a90af626957659b5-77a8-4f61-a4d4-9fcb591787af2025-04-02WarningsExact identifier
spl set id: 957659b5-77a8-4f61-a4d4-9fcb591787af

Reported adverse events (FAERS/openFDA)#

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