FDA.reportPublic FDA data

Rilakkuma Aloe Vera Scented

Manufacturer
Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch
Effective date
2022-09-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:50:40

Label at a glance#

ProductRilakkuma Aloe Vera Scented
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Rub a dime sized amount into hands

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacterial on hands

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a 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 sized amount into hands

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, carbomer, triethanolamine, glycerol, aloe extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN2
1047755ethanol 0.75 ML/ML Topical SolutionSCD2
1047755ethanol 75 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75112-009-012023-07-28C16284748780-1e4f33bdf-b3ab-d8a0-e053-dadaa90a6e4e75112-009 Rilakkuma
75112-009-012022-09-14C16284748780-1e4f33bdf-b3ab-d8a0-e053-dadaa90a6e4e75112-009 Rilakkuma
75112-009-012022-07-29C16284748780-1e4f33bdf-b3ab-d8a0-e053-dadaa90a6e4e75112-009 Rilakkuma

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75112-009-01Rilakkuma Aloe Vera Scented30 mL in 1 BOTTLESOLUTION302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75112-009RILAKKUMA ALOE VERA SCENTED (ALCOHOL) SOLUTION [ZHEJIANG SHENYING TECHNOLOGY CO., LTD. JIAOJIANG BRANCH]2Legacy NDC, 1 package rows20220916_8b7b661d-918e-4403-86e5-d16c297fbc7c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75112-00975112-009-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CARBOMER 934Z135WT9208IACT
TROLAMINE9O3K93S3TKIACT
GLYCEROL FORMAL3L7GR2604EIACT
ALOEV5VD430YW9IACT
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
e8b0673e-ed19-6af7-e053-2a95a90adeaf8b7b661d-918e-4403-86e5-d16c297fbc7c2022-09-15WarningsExact identifier
spl id: e8b0673e-ed19-6af7-e053-2a95a90adeaf
spl set id: 8b7b661d-918e-4403-86e5-d16c297fbc7c

Reported adverse events (FAERS/openFDA)#

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