Sani-Pen

Manufacturer: Natural Trends, LLC
Effective date: 2020-08-14
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:24:37

Label at a glance#

ProductSani-Pen

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Storage and handling

Do not store above 105° F.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame

For external use only.

When using this product

Do not use in eyes. In case of contact with eyes, rinse with water.

Stop use & ask a doctor if irritation & redness develop & persist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help soon.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

Do not store above 105° F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Triethanolamine, Glycerin, Propylene glycol, Aloe Barbadensis, Vitamine E, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	1
582753	ethanol 0.7 ML/ML Topical Solution	SCD	1
582753	ethanol 70 % Topical Solution	SY	1
582753	ethyl alcohol 70 % Topical Solution	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7792dadb-52b6-46b6-8fdf-80b1171065b5	Product name	1	20180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
20590-003-01	2022-01-28	C162847	48780-1	d6a99b39-e07e-a426-e053-dadaa90af4c2	0ce6fbc8-52b2-4d8e-a1cb-fb0437cace15
20590-003-02	2022-01-28	C162847	48780-1	d6a99b39-e07e-a426-e053-dadaa90af4c2	0ce6fbc8-52b2-4d8e-a1cb-fb0437cace15

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
20590-003-01	Sani-Pen	10 mL in 1 TUBE	LIQUID	10		1
20590-003-02	Sani-Pen	15 mL in 1 TUBE	LIQUID	15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
20590-003	SANI-PEN (ALCOHOL) LIQUID [NATURAL TRENDS, LLC]	1	Legacy NDC, 2 package rows	20200814_0ce6fbc8-52b2-4d8e-a1cb-fb0437cace15.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Sani-Pen
Alcohol
ALOE
PROPYLENE GLYCOL
TROLAMINE
.ALPHA.-TOCOPHEROL
GLYCERIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
20590-003	20590-003-01, 20590-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
ALOE	V5VD430YW9	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
TROLAMINE	9O3K93S3TK	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
GLYCERIN	PDC6A3C0OX	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
ba2e7624-dea9-4fa2-83cc-73946284b941			0ce6fbc8-52b2-4d8e-a1cb-fb0437cace15	2020-08-14	Warnings	Exact identifier spl id: ba2e7624-dea9-4fa2-83cc-73946284b941 spl set id: 0ce6fbc8-52b2-4d8e-a1cb-fb0437cace15

Reported adverse events (FAERS/openFDA)#

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