Sumikkogurashi Aloe Vera Scented

Manufacturer
JIANGSU HANHE DAILY CHEMICALS CO., LTD.
Effective date
2023-03-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:54:28

Label at a glance#

ProductSumikkogurashi Aloe Vera Scented
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Rub a dime sied amount into hands

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bateria on hands

Warnings

WARNINGS SECTION

For external use only.

Non Medical. Flammable. Keep away from high heat or flame

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water

OTC - STOP USE SECTION

Stop use and ask doctor if irritation occurs and redness develops or increases.

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

  • Rub a dime sied amount into hands

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerol, Aloe Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN3
1305100ethanol 0.75 ML/ML Topical GelSCD3
1305100ethanol 75 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73027-215-01Sumikkogurashi Aloe Vera Scented30 mL in 1 BOTTLEGEL303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73027-215SUMIKKOGURASHI ALOE VERA SCENTED (ALCOHOL) GEL [JIANGSU HANHE DAILY CHEMICALS CO., LTD.]3Legacy NDC, 1 package rows20230316_4fa7fb5c-8ee6-4ff4-b7c9-13621b50da91.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
73027-21573027-215-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
f6f149ea-384b-2718-e053-6394a90a25de4fa7fb5c-8ee6-4ff4-b7c9-13621b50da912023-03-14WarningsExact identifier
spl id: f6f149ea-384b-2718-e053-6394a90a25de
spl set id: 4fa7fb5c-8ee6-4ff4-b7c9-13621b50da91

Reported adverse events (FAERS/openFDA)#

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