FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
Huizhou Yiyani Cosmetic Co., Ltd.
Effective date
2020-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:33

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry Children under 6 years of age should be supervised when using this product.

Storage and handling

store below106°F(41°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame
Forexternal use only.

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

OTC - STOP USE SECTION

Stop use and ask doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Kepp out of reach for children. if swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry
Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

store below106°F(41°C)
May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerine, Isopropyl Alcohol, Propylene glycol, Carbomer, Triethanolamine, Parfum, aqua

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

001001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59541-541-012022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-022022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-032022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-042022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-052022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-062022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-072022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-082022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-092022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER
59541-541-102022-01-28C16284748780-1d6a99b39-c4ed-a426-e053-dadaa90af4c2HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59541-541-01HAND SANITIZER15 mL in 1 BOTTLEGEL151
59541-541-02HAND SANITIZER20 mL in 1 BOTTLEGEL201
59541-541-03HAND SANITIZER30 mL in 1 BOTTLEGEL301
59541-541-04HAND SANITIZER50 mL in 1 BOTTLEGEL501
59541-541-05HAND SANITIZER100 mL in 1 BOTTLEGEL1001
59541-541-06HAND SANITIZER250 mL in 1 BOTTLEGEL2501
59541-541-07HAND SANITIZER300 mL in 1 BOTTLEGEL3001
59541-541-08HAND SANITIZER500 mL in 1 BOTTLEGEL5001
59541-541-09HAND SANITIZER1000 mL in 1 BOTTLEGEL10001
59541-541-10HAND SANITIZER5000 mL in 1 BOTTLEGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59541-541HAND SANITIZER GEL [HUIZHOU YIYANI COSMETIC CO., LTD.]1Legacy NDC, 10 package rows20200725_ab02e7a6-9720-e346-e053-2a95a90a1414.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59541-54159541-541-01, 59541-541-02, 59541-541-03, 59541-541-04, 59541-541-05, 59541-541-06, 59541-541-07, 59541-541-08, 59541-541-09, 59541-541-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
METHYL BENZOATE6618K1VJ9TIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
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
ab02e7a6-9712-e346-e053-2a95a90a1414ab02e7a6-9720-e346-e053-2a95a90a14142020-07-22WarningsExact identifier
spl id: ab02e7a6-9712-e346-e053-2a95a90a1414
spl set id: ab02e7a6-9720-e346-e053-2a95a90a1414

Reported adverse events (FAERS/openFDA)#

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