KidzStuff Hand Sanitizer

Manufacturer: JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Effective date: 2018-01-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:54:11

Label at a glance#

ProductKidzStuff Hand Sanitizer

Active ingredientALCOHOL

Label structure6 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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

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 skin irritation develops.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, immediately flush with water and call a doctor.
avoid contact with broken skin.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water, glycerin, triethanolamine, carbomer, aloe essence

Product Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247835	ethanol 62 % Topical Solution	PSN	1
247835	ethanol 0.62 ML/ML Topical Solution	SCD	1
247835	ethanol 62 % Topical Solution	SY	1
247835	ethyl alcohol 62 % Topical Solution	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71734-204-01	KidzStuff Hand Sanitizer	2 g in 1 BOTTLE	LIQUID	2		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71734-204	KIDZSTUFF HAND SANITIZER (ALCOHOL) LIQUID [JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.]	1	Current NDC, Legacy NDC, 1 package rows	20180119_7ecf92e5-0ad6-41f0-bd02-2f79acb2b722.zip

Products#

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

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

KidzStuff Hand Sanitizer
ALCOHOL
ALOE VERA LEAF
GLYCERIN
PROPYLENE GLYCOL
TOCOPHEROL
TROLAMINE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71734-204	71734-204-01

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 VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
TOCOPHEROL	R0ZB2556P8	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
KidzStuff Hand Sanitizer	ALCOHOL	JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.	7ecf92e5-0ad6-41f0-bd02-2f79acb2b722	2018-01-17	Warnings	Exact identifier ndc (package): 71734-204-01 ndc (product): 71734-204 ndc11 (package): 71734020401 spl id: 7b66fbd8-0469-4370-b7d0-126ab69d4d49 spl set id: 7ecf92e5-0ad6-41f0-bd02-2f79acb2b722

Reported adverse events (FAERS/openFDA)#

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