SHICELLE Hand Sanitizer

Manufacturer: YIWU ANKO COSMETICS CO., LTD
Effective date: 2020-05-04
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:09:40

Label at a glance#

ProductSHICELLE Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To reduce bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only -hands

Flammable. Keep away from fire or flame

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and condistion persists for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub until dry without wiping
For children under 6, use only under adult supervision
Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, olive oil PEG-7 ester, acrylates /C10-30 alkyl acrylate cross polymer, triethanolamine, fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1047755	ethanol 75 % Topical Solution	PSN	1
1047755	ethanol 0.75 ML/ML Topical Solution	SCD	1
1047755	ethanol 75 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77292-001-01	2022-01-28	C162847	48780-1	d6a99b39-7170-a426-e053-dadaa90af4c2	b00b0c3e-2a45-4c53-9222-037abdfe85dc
77292-001-02	2022-01-28	C162847	48780-1	d6a99b39-7170-a426-e053-dadaa90af4c2	b00b0c3e-2a45-4c53-9222-037abdfe85dc
77292-001-03	2022-01-28	C162847	48780-1	d6a99b39-7170-a426-e053-dadaa90af4c2	b00b0c3e-2a45-4c53-9222-037abdfe85dc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77292-001-01	SHICELLE Hand Sanitizer	50 mL in 1 BOTTLE	SOLUTION	50	1
77292-001-02	SHICELLE Hand Sanitizer	300 mL in 1 BOTTLE	SOLUTION	300	1
77292-001-03	SHICELLE Hand Sanitizer	500 mL in 1 BOTTLE	SOLUTION	500	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77292-001	SHICELLE HAND SANITIZER (ALCOHOL) SOLUTION [YIWU ANKO COSMETICS CO., LTD]	1	Legacy NDC, 3 package rows	20200505_b00b0c3e-2a45-4c53-9222-037abdfe85dc.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

SHICELLE Hand Sanitizer
Alcohol
GLYCERIN
WATER
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77292-001	77292-001-01, 77292-001-02, 77292-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	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
a4df314e-bd5b-7e5c-e053-2a95a90afc25			b00b0c3e-2a45-4c53-9222-037abdfe85dc	2020-05-04	Warnings	Exact identifier spl id: a4df314e-bd5b-7e5c-e053-2a95a90afc25 spl set id: b00b0c3e-2a45-4c53-9222-037abdfe85dc

Reported adverse events (FAERS/openFDA)#

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