ACS GOLDEN TOUCH ANTISEPTIC HAND SANITIZER

Manufacturer
American Chemical Systems II, LLC
Effective date
2022-03-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:06:22

Label at a glance#

ProductACS GOLDEN TOUCH ANTISEPTIC HAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
• for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame

For external use only

Do not use

• in children less than 2 months of age
• on open skin wounds


When using this product
• do not get into eyes. In case of contact, rinse eyes thoroughly with water


Stop use and ask a doctor if

• irritation or redness develop
• condition persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F)
• avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, hydroxyethyl cellulose, fragrance, glycerin, betaine, propanediol, sodium hydroxide, aloe vera (Aloe barbadensis) leaf juice, tocopheryl acetate (vitamin E acetate)

Questions?

OTC - QUESTIONS SECTION

+1-800-889-3489
You may also report serious side effects to this phone number.
Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

♦ With Moisturizers, Aloe, and Vitamin E
♦ Lemongrass Fragrance
♦ Skin Conditioners
♦ Quick Dry
♦ Smooth Silky Feel

Manufactured by:
AMERICAN CHEMICAL SYSTEMS II, LLC
3505 W. 29th Street South,
Wichita, Kansas 67217

READ PRECAUTIONS CAREFULLY

Safety Data Sheet (SDS) is available at:

americanchemicalsystemsii.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75044-261-572022-03-11C16284748780-1d6a99b39-59d9-a426-e053-dadaa90af4c2ACS GOLDEN TOUCH ANTISEPTIC HAND SANITIZER
75044-261-572022-01-28C16284748780-1d6a99b39-59d9-a426-e053-dadaa90af4c2ACS GOLDEN TOUCH ANTISEPTIC HAND SANITIZER

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75044-26175044-261-57

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
7c5c0cd5-d917-4c6f-831c-15d09634de7fa7316dae-186b-4bea-b5a0-24bf1d7e32072022-03-11WarningsExact identifier
spl id: 7c5c0cd5-d917-4c6f-831c-15d09634de7f
spl set id: a7316dae-186b-4bea-b5a0-24bf1d7e3207

Reported adverse events (FAERS/openFDA)#

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