Yangzhou Sanitizer Gel

Manufacturer: Yangzhou Huangxuan Daily Chemical Co Ltd
Effective date: 2020-08-27
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:06

Label at a glance#

ProductBaishichen

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

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

Storage and handling

Avoid freezing and excessive heat above 40C (104F) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

in children less than 2 months of age
on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

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

Other information

STORAGE AND HANDLING SECTION

Avoid freezing and excessive heat above 40C (104F)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, glycerin, triethanolamine, water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 mL NDC:79808-111-03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79808-111-01	2022-01-28	C162847	48780-1	d6a99b39-5ffd-a426-e053-dadaa90af4c2	Yangzhou Sanitizer Gel
79808-111-02	2022-01-28	C162847	48780-1	d6a99b39-5ffd-a426-e053-dadaa90af4c2	Yangzhou Sanitizer Gel
79808-111-03	2022-01-28	C162847	48780-1	d6a99b39-5ffd-a426-e053-dadaa90af4c2	Yangzhou Sanitizer Gel
79808-111-04	2022-01-28	C162847	48780-1	d6a99b39-5ffd-a426-e053-dadaa90af4c2	Yangzhou Sanitizer Gel
79808-111-05	2022-01-28	C162847	48780-1	d6a99b39-5ffd-a426-e053-dadaa90af4c2	Yangzhou Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
79808-111-01	Baishichen	30 mL in 1 BOTTLE	GEL	30	1
79808-111-02	Baishichen	60 mL in 1 BOTTLE	GEL	60	1
79808-111-03	Baishichen	100 mL in 1 BOTTLE	GEL	100	1
79808-111-04	Baishichen	300 mL in 1 BOTTLE	GEL	300	1
79808-111-05	Baishichen	500 mL in 1 BOTTLE	GEL	500	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79808-111	BAISHICHEN (HAND SANITIZER GEL) GEL [YANGZHOU HUANGXUAN DAILY CHEMICAL CO LTD]	1	Legacy NDC, 5 package rows	20200828_addedbf1-71ec-1599-e053-2995a90aa68d.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Baishichen
Hand Sanitizer Gel
CARBOMER INTERPOLYMER TYPE C (ALLYL SUCROSE CROSSLINKED)
GLYCERIN
TRIETHANOLAMINE PHOSPHATE
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79808-111	79808-111-01, 79808-111-02, 79808-111-03, 79808-111-04, 79808-111-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER INTERPOLYMER TYPE C (ALLYL SUCROSE CROSSLINKED)	U990QE4LKP	IACT
GLYCERIN	PDC6A3C0OX	IACT
TRIETHANOLAMINE PHOSPHATE	4GH264P17A	IACT
WATER	059QF0KO0R	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
addedbf1-71de-1599-e053-2995a90aa68d			addedbf1-71ec-1599-e053-2995a90aa68d	2020-08-27	Warnings	Exact identifier spl id: addedbf1-71de-1599-e053-2995a90aa68d spl set id: addedbf1-71ec-1599-e053-2995a90aa68d

Reported adverse events (FAERS/openFDA)#

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