Be Smart Get Prepared Hand Sanitizer

Manufacturer: Total Resources International, Inc
Effective date: 2024-07-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:14:53

Label at a glance#

ProductBe Smart Get Prepared Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

For handwashing to decrease bacteria on skin without soap and water.

Dosage and administration

wet hands & wrists thoroughly with product and allow to dry without wiping

Contacts and useful links#

Websitewww.trikits.com

www.trikits.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 66.5%(v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on skin without soap and water.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

Do not use in eyes, if this happens, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use, ask a doctor if irritation develops and persists for 72 hours.

If ingested, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands & wrists thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

Principal Display Panel – 1 mL Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BE SMART

GET PREPARED®

HAND SANITIZER

0.05 oz [1.50 g]

Kills 99.9% of Germs

Aloe Vera • Single Use

Made in USA

Manufactured for Total Resources Intl. Inc

Walnut, California 91789

www.trikits.com • 00-SAN-9600 Rev.01

NDC 55550-106-02

Principal Display Panel – 1 mL Pouch Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616762	ethanol 66.5 % Topical Gel	PSN	1
616762	ethanol 0.665 ML/ML Topical Gel	SCD	1
616762	ethanol 66.5 % Topical Gel	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55550-106-02	Be Smart Get Prepared Hand Sanitizer	1 mL in 1 POUCH	GEL	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55550-106	BE SMART GET PREPARED HAND SANITIZER (ALCOHOL) GEL [TOTAL RESOURCES INTERNATIONAL, INC]	1	Current NDC, Legacy NDC, 1 package rows	20240709_e7930ec4-6920-4abb-adce-8cc4de44801d.zip

Products#

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

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

Be Smart Get Prepared Hand Sanitizer
Alcohol
ALOE
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
D&C GREEN NO. 5
D&C YELLOW NO. 10
TROLAMINE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55550-106	55550-106-02

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
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
D&C GREEN NO. 5	8J6RDU8L9X	IACT
D&C YELLOW NO. 10	35SW5USQ3G	IACT
TROLAMINE	9O3K93S3TK	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
Be Smart Get Prepared Hand Sanitizer	ALCOHOL	Total Resources International, Inc	e7930ec4-6920-4abb-adce-8cc4de44801d	2024-07-02	Warnings	Exact identifier ndc (package): 55550-106-02 ndc (product): 55550-106 ndc11 (package): 55550010602 spl id: 8d360c0d-a4f8-4dac-8e76-922a5f05d510 spl set id: e7930ec4-6920-4abb-adce-8cc4de44801d

Reported adverse events (FAERS/openFDA)#

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