FDA.reportPublic FDA data

Phoenix Hand Sanitizer Gel

Manufacturer
THANH CONG PHARMACEUTICAL AND TRADING CO.,LTD
Effective date
2020-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:09

Label at a glance#

ProductPhoenix Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• Help to clean hand quickly. • Resist bacteria without water, deodorizer.

Dosage and administration

• Use about 5 ml of solution, massage lightly whole hand that need to be cleaned until dry. • Do not need to wash again with water.

Storage and handling

• Store between 15-30°C (59-86°F). • Avoid freezing and excessive heat above 40°C (104°F).

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70% + 3%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• Help to clean hand quickly.

• Resist bacteria without water, deodorizer.

WARNINGS SECTION

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

Do not use 

• In children less than 2 months of age.

• On open skin wounds.

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.

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 at 1 - 800 -222 - 1222.

Directions

DOSAGE & ADMINISTRATION SECTION

• Use about 5 ml of solution, massage lightly whole hand that need to be cleaned until dry.

• Do not need to wash again with water.

Other information

STORAGE AND HANDLING SECTION

• Store between 15-30°C (59-86°F).

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

INACTIVE INGREDIENT SECTION

Inactive ingredients: Carbomer, Triethanolamine (TEA), Water.

SPL UNCLASSIFIED SECTION

Alcohol 70%

• Clean hands quickly

• Resist bacteria

• Deodorizer

DO NOT DRINK

NO NEED TO WASH AGAIN WITH WATER

Manufactured & packed for:

AM PACKAGING CORPORATION LTD

233 BROADWAY, SUITE 2040, NEW YORK, NY 10279, USA

Email: orders@ampccorp.com

Made in Viet Nam

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Phoenix1Phoenix1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80666-555-502022-01-28C16284748780-1d6a99b39-964b-a426-e053-dadaa90af4c2Phoenix Hand Sanitizer Gel
80666-555-552022-01-28C16284748780-1d6a99b39-964b-a426-e053-dadaa90af4c2Phoenix Hand Sanitizer Gel
80666-555-562022-01-28C16284748780-1d6a99b39-964b-a426-e053-dadaa90af4c2Phoenix Hand Sanitizer Gel
80666-555-582022-01-28C16284748780-1d6a99b39-964b-a426-e053-dadaa90af4c2Phoenix Hand Sanitizer Gel
80666-555-802022-01-28C16284748780-1d6a99b39-964b-a426-e053-dadaa90af4c2Phoenix Hand Sanitizer Gel
80666-555-852022-01-28C16284748780-1d6a99b39-964b-a426-e053-dadaa90af4c2Phoenix Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80666-555-50Phoenix Hand Sanitizer Gel1000 mL in 1 BOTTLEGEL10001
80666-555-55Phoenix Hand Sanitizer Gel500 mL in 1 BOTTLEGEL5001
80666-555-56Phoenix Hand Sanitizer Gel3800 mL in 1 CANGEL38001
80666-555-58Phoenix Hand Sanitizer Gel5000 mL in 1 CANGEL50001
80666-555-80Phoenix Hand Sanitizer Gel250 mL in 1 BOTTLEGEL2501
80666-555-85Phoenix Hand Sanitizer Gel100 mL in 1 BOTTLEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80666-555PHOENIX HAND SANITIZER GEL (ETHYL ALCOHOL) GEL [THANH CONG PHARMACEUTICAL AND TRADING CO.,LTD]1Legacy NDC, 6 package rows20201007_f1153eee-b624-407d-bd2c-2ba864356a63.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
80666-55580666-555-85, 80666-555-80, 80666-555-55, 80666-555-50, 80666-555-56, 80666-555-58

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
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT

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
1224bc76-eaf8-4676-934e-0f1db8fe725af1153eee-b624-407d-bd2c-2ba864356a632020-10-05WarningsExact identifier
spl id: 1224bc76-eaf8-4676-934e-0f1db8fe725a
spl set id: f1153eee-b624-407d-bd2c-2ba864356a63

Reported adverse events (FAERS/openFDA)#

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