Hand Sanitizer

Manufacturer
Ganzhou Yixin Cosmetics Co ,Ltd
Effective date
2020-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:10

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands throughly with product and allow to dry without wiping

Storage and handling

/

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help decreasebacteria on the skine recommended for repeat use

Warnings

WARNINGS SECTION

For extemal use only. .Flammable,.Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

/

OTC - WHEN USING SECTION

In case of contact flush eyes with water.Avoid contact with eyes and nose

OTC - STOP USE SECTION

Stop use and ask a doctorif irritation or rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.These may be signs of a serious conditionIf swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands throughly with product and allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

  • /

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, CarbomerTriethanolamine, Fragrance

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78496-006-01Hand Sanitizer15 mL in 1 BOTTLEGEL151
78496-006-02Hand Sanitizer30 mL in 1 BOTTLEGEL301
78496-006-03Hand Sanitizer50 mL in 1 BOTTLEGEL501
78496-006-04Hand Sanitizer60 mL in 1 BOTTLEGEL601
78496-006-05Hand Sanitizer120 mL in 1 BOTTLEGEL1201
78496-006-06Hand Sanitizer250 mL in 1 BOTTLEGEL2501
78496-006-07Hand Sanitizer100 mL in 1 BOTTLEGEL1001
78496-006-08Hand Sanitizer500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78496-006HAND SANITIZER GEL [GANZHOU YIXIN COSMETICS CO ,LTD]1Legacy NDC, 8 package rows20200605_a73ce3c5-0f5d-ae31-e053-2a95a90ab4ef.zip

Products#

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

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
a73ce7e3-a895-5858-e053-2a95a90a0c07a73ce3c5-0f5d-ae31-e053-2a95a90ab4ef2020-06-04WarningsExact identifier
spl id: a73ce7e3-a895-5858-e053-2a95a90a0c07
spl set id: a73ce3c5-0f5d-ae31-e053-2a95a90ab4ef

Reported adverse events (FAERS/openFDA)#

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