DR. WRIGHTS ANTISEPTIC HAND SANITIZER

Manufacturer: Moeller Brew Barn LLC
Effective date: 2020-03-28
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:06:05

Label at a glance#

ProductDR. WRIGHTS ANTISEPTIC HAND SANITIZER

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

hand sanitizer to decrease 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 80% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

hand sanitizer to decrease 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 and 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

glycerin, hydrogen peroxide, water

Questions? +1-419-925-3030

OTC - QUESTIONS SECTION

You may also report serious side effects to this phone number.

Mon-Fri 9:00 AM - 5:00 PM

SPL UNCLASSIFIED SECTION

MANUFACTURED BY: MOELLER BREW BARN, 8016 MARION DRIVE, MARIA STEIN, OH-45860

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Wrightfnl

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039339	ethanol 80 % Topical Solution	PSN	1
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	1
1039339	ethanol 80 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74158-001-01	2022-01-28	C162847	48780-1	d6a99b39-3a50-a426-e053-dadaa90af4c2	DR. WRIGHT'S ANTISEPTIC HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74158-001-01	DR. WRIGHTS ANTISEPTIC HAND SANITIZER	177 mL in 1 BOTTLE, PLASTIC	LIQUID	177		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74158-001	DR. WRIGHTS ANTISEPTIC HAND SANITIZER (ALCOHOL) LIQUID [MOELLER BREW BARN LLC]	1	Legacy NDC, 1 package rows	20200413_a6e27e78-cd0a-4609-921c-637831889f64.zip

Products#

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

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

DR. WRIGHTS ANTISEPTIC HAND SANITIZER
Alcohol
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74158-001	74158-001-01

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
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
54de46bc-1210-4b3a-998f-a06261cde2d9			a6e27e78-cd0a-4609-921c-637831889f64	2020-03-28	Warnings	Exact identifier spl id: 54de46bc-1210-4b3a-998f-a06261cde2d9 spl set id: a6e27e78-cd0a-4609-921c-637831889f64

Reported adverse events (FAERS/openFDA)#

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