Pure Choice Instant Hand Sanitizer

Manufacturer: Shanghai Medical Instruments Co.,Ltd
Effective date: 2020-04-27
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 23:08:24

Label at a glance#

ProductPure Choice Instant Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

1)Put enough product in your palm to cover hands and rub hands together briskly until dry. 2) Children under 6 years of age should be supervised when using

Contacts and useful links#

PhoneLabel contact1-866-222-3181

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use:

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame
For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts

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

1)Put enough product in your palm to cover hands and rub hands together briskly until dry. 2) Children under 6 years of age should be supervised when using

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Water, Carbomer, aloe extraction, Triethanolamine, Ammonium Lauryl Sulfate, Hyaluronic Acid, Aloe Extract, Parfum

OTC - QUESTIONS SECTION

Question? 1-866-222-3181.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	3
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	3
1305100	ethanol 75 % Topical Gel	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74854-001-26	2021-07-23	C162847	48780-1	c7ccaba7-290a-fd44-e053-dadaa90aa01b	Pure Choice Instant Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74854-001-26	Pure Choice Instant Hand Sanitizer	260 mL in 1 BOTTLE	GEL	260		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74854-001	PURE CHOICE INSTANT HAND SANITIZER (ALCOHOL) GEL [SHANGHAI MEDICAL INSTRUMENTS CO.,LTD]	3	Legacy NDC, 1 package rows	20200428_cd1d36b7-cfe1-48cb-88d7-f00f0e30e60c.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Pure Choice Instant Hand Sanitizer
ALCOHOL
GLYCERIN
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
AMMONIUM LAURYL SULFATE
HYALURONIC ACID
ALOE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74854-001	74854-001-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
AMMONIUM LAURYL SULFATE	Q7AO2R1M0B	IACT
HYALURONIC ACID	S270N0TRQY	IACT
ALOE	V5VD430YW9	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
a446ab96-9fcb-1a08-e053-2a95a90a7171			cd1d36b7-cfe1-48cb-88d7-f00f0e30e60c	2020-04-27	Warnings	Exact identifier spl id: a446ab96-9fcb-1a08-e053-2a95a90a7171 spl set id: cd1d36b7-cfe1-48cb-88d7-f00f0e30e60c

Reported adverse events (FAERS/openFDA)#

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