DOUNDRINS DISTILLING HAND SANITIZER

Manufacturer: Doundrins Distilling
Effective date: 2020-04-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:46

Label at a glance#

ProductDOUNDRINS DISTILLING HAND SANITIZER

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

-to decrease bacteria on the skin that could cause disease -recommended for repeated use

Dosage and administration

-wet hands thoroughly with product and allow to dry without wiping. -for children under 6, use only under adult supervision -not recommended for infants

Storage and handling

-do not store above 105 degrees farenheit -may discolor some fabrics -harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

-to decrease bacteria on the skin that could cause disease -recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable. Keep away from heat and flame.

When using this product

-keep out of eyes. In case of contact with eyes, flush thoroughly with water. -avoid contact with broken skin.

-do not inhale or ingest

Stop use and ask a doctor if

-irritation or redness develops -condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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. -for children under 6, use only under adult supervision -not recommended for infants

Other Information

STORAGE AND HANDLING SECTION

-do not store above 105 degrees farenheit -may discolor some fabrics -harmful to wood finishes and plastics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerol, peroxide, water

SPL UNCLASSIFIED SECTION

Produced and Bottled by

Doundrins Distilling, Cottage Grove, WI

doundrinsdistilling.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitled

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74547-001-04	2022-01-28	C162847	48780-1	d6a99b39-3bb6-a426-e053-dadaa90af4c2	DOUNDRINS DISTILLING HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74547-001-04	DOUNDRINS DISTILLING HAND SANITIZER	3.79 L in 1 BOTTLE, PLASTIC	LIQUID	3.79		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74547-001	DOUNDRINS DISTILLING HAND SANITIZER (ETHYL ALCOHOL) LIQUID [DOUNDRINS DISTILLING]	1	Legacy NDC, 1 package rows	20200430_7e99cf5a-bd94-4e2d-9756-b73007745d9b.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

DOUNDRINS DISTILLING HAND SANITIZER
Ethyl alcohol
ALCOHOL
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74547-001	74547-001-04

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 · Source PDF

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
fa4ea841-921f-414c-ae3a-e3efca38e5a5			7e99cf5a-bd94-4e2d-9756-b73007745d9b	2020-04-21	Warnings	Exact identifier spl id: fa4ea841-921f-414c-ae3a-e3efca38e5a5 spl set id: 7e99cf5a-bd94-4e2d-9756-b73007745d9b

Reported adverse events (FAERS/openFDA)#

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