First Hand Hand Sanitizer

Manufacturer: South Tenth Development, LLC
Effective date: 2020-06-15
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:17:44

Label at a glance#

ProductFirst Hand Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

Reduce bacteria on the skin. Recommended for repeated use

Dosage and administration

- Place enough to cover both hands in the palm, and rub hands together until dry. - Children under 6 years of age should be supervised by an adult when applying this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Reduce bacteria on the skin. Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.

Flammable Keep away from fire, flame, or sparks

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact, rinse eyes thoroughly with water

Stop use & ask a doctor

OTC - STOP USE SECTION

If irritation or rash appears on the skin.

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

- Place enough to cover both hands in the palm, and rub hands together until dry.
- Children under 6 years of age should be supervised by an adult when applying this product.

Other Information

SPL UNCLASSIFIED SECTION

- Store below 105°F.
- May discolor certain fabrics or surfaces.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Distilled water, glycerol, hydrogen peroxide, denatonium benzoate.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039339	ethanol 80 % Topical Solution	PSN	2
1039339	ethanol 0.8 ML/ML Topical Solution	SCD	2
1039339	ethanol 80 % Topical Solution	SY	2

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
78705-000-00	2022-01-28	C162847	48780-1	d6a99b39-dbb2-a426-e053-dadaa90af4c2	"First Hand" Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78705-000-00	First Hand Hand Sanitizer	295 mL in 1 BOTTLE	LIQUID	295		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78705-000	FIRST HAND HAND SANITIZER (ALCOHOL) LIQUID [SOUTH TENTH DEVELOPMENT, LLC]	2	Legacy NDC, 1 package rows	20200616_195b802c-f79c-4e7b-aa74-eb897771f182.zip

Products#

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

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

First Hand Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
HYDROGEN PEROXIDE
DENATONIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78705-000	78705-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT
ALCOHOL	3K9958V90M	ACTIB

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
a820c93b-ecf7-61f5-e053-2995a90a9b06			195b802c-f79c-4e7b-aa74-eb897771f182	2020-06-15	Warnings	Exact identifier spl id: a820c93b-ecf7-61f5-e053-2995a90a9b06 spl set id: 195b802c-f79c-4e7b-aa74-eb897771f182

Reported adverse events (FAERS/openFDA)#

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