FDA.reportPublic FDA data

Chinese Mugwort Antibacterial Sprays of Yishiyuan

Manufacturer
Hubei Yishiyuan Chinese Mugwort Biotechnology Co., Ltd. | A03 Lab of BTS
Effective date
2020-04-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:09

Label at a glance#

ProductChinese Mugwort Antibacterial Sprays of Yishiyuan
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Spray on your hands or skin when needed.

Storage and handling

Store in a cool, dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v. Purpose: Antiseptic.

Kill staphylococcus aureus, escherichia coli, pseudomonas aeruginosa, and candida albicans (ATCC10231).

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.

Suitable for daily hand and skin disinfection.

Warnings

WARNINGS SECTION

1. External use only.

2. Flammable, away from fire source.

3. Keep out of reach of children.

Do not use

OTC - DO NOT USE SECTION

  • on children less than 2 months of age
  • on open skin wounds
  • in the eyes. in case of contact, rinse eyes thoroughly with water

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and persist 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

Spray on your hands or skin when needed.

Other information

STORAGE AND HANDLING SECTION

Store in a cool, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Essential Oil of Chinese Mugwort, Benzyldodecyldimethylammonium Bromide.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN1
2286295ethanol 0.75 ML/ML Topical SpraySCD1
2286295ethanol 75 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75507-1011-62021-07-23C16284748780-1c7ccaba7-0fc0-fd44-e053-dadaa90aa01bYiShiYuan, Chinese Mugwort Antibacterial Sprays, Liquid, 100mL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75507-1011-1Chinese Mugwort Antibacterial Sprays of Yishiyuan100 mL in 1 BOTTLE, SPRAYLIQUID1001
75507-1011-6Chinese Mugwort Antibacterial Sprays of Yishiyuan100 in 1 BOXLIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75507-1011CHINESE MUGWORT ANTIBACTERIAL SPRAYS OF YISHIYUAN (HAND SANITIZER) LIQUID [HUBEI YISHIYUAN CHINESE MUGWORT BIOTECHNOLOGY CO., LTD.]1Legacy NDC, 2 package rows20200427_a43d76a0-24ae-4fc8-e053-2995a90aac17.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75507-101175507-1011-1, 75507-1011-6

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
NameUNIIKind
ARTEMISIA ARGYI LEAF2JYC99Q0WZIACT
BENZODODECINIUM BROMIDEIRY12B2TQ6IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a43d76a0-24af-4fc8-e053-2995a90aac17a43d76a0-24ae-4fc8-e053-2995a90aac172020-04-24WarningsExact identifier
spl id: a43d76a0-24af-4fc8-e053-2995a90aac17
spl set id: a43d76a0-24ae-4fc8-e053-2995a90aac17

Reported adverse events (FAERS/openFDA)#

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