FDA.reportPublic FDA data

PAMELA HAND SANITIZER

Manufacturer
YESROAD COSMETICS CO.,LTD
Effective date
2020-08-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:29:01

Label at a glance#

ProductPAMELA HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

alcohol

INACTIVE INGREDIENT SECTION

Water
Glycerin

Carbomer

Helianthus Annuus Hybrid (Sunflower) oil
Chamomilla Recutita (Matricaria) Extract
Butylene Glycol

Aloe Barbadensis Leaf Extract

Butylene Glycol

1,2-Hexanediol

Aminomethyl Propanol

OTC - PURPOSE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

wet hands thoroughly with product and allow to dry without wiping

WARNINGS SECTION

Flammable, keep away from fire and flames
Fot external use only.

DOSAGE & ADMINISTRATION SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78924-0003-12022-01-28C16284748780-1d6a99b39-7aa4-a426-e053-dadaa90af4c2a7f1093c-4bbc-216d-e053-2995a90adb2e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78924-0003-1PAMELA HAND SANITIZER500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78924-0003PAMELA HAND SANITIZER (ALCOHOL) GEL [YESROAD COSMETICS CO.,LTD]2Legacy NDC, 1 package rows20200911_a7f1093c-4bbc-216d-e053-2995a90adb2e.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78924-000378924-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
1,2-HEXANEDIOLTR046Y3K1GIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MATRICARIA RECUTITAG0R4UBI2ZZIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 9404Q93RCW27EIACT
SUNFLOWER OIL3W1JG795YIIACT

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
adf64058-4d43-aa3c-e053-2a95a90a656ba7f1093c-4bbc-216d-e053-2995a90adb2e2020-08-28WarningsExact identifier
spl id: adf64058-4d43-aa3c-e053-2a95a90a656b
spl set id: a7f1093c-4bbc-216d-e053-2995a90adb2e

Reported adverse events (FAERS/openFDA)#

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