FDA.reportPublic FDA data

PURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER

Manufacturer
Ester Co., Ltd.
Effective date
2020-07-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:39

Label at a glance#

ProductPURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZERPURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74004-025-202022-01-28C16284748780-1d6a99b39-f7b3-a426-e053-dadaa90af4c2[Ester Co., Ltd.-PURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER] 25 mL pouch x 20 EA in box

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74004-025-01PURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER25 mL in 1 POUCHGEL251
74004-025-20PURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER20 in 1 BOXGEL201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74004-025PURIFACE ANTI-BACTERIAL MOISTURIZING HAND SANITIZER (ETHYL ALCOHOL) GEL [ESTER CO., LTD.]1Legacy NDC, 2 package rows20200709_a9ea4c97-ef70-e140-e053-2995a90a97b6.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
74004-02574004-025-01, 74004-025-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
COPTIS CHINENSIS ROOTCXS4LJR7ELIACT
CARBOMER INTERPOLYMER TYPE A (55000 CPS)59TL3WG5COIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT

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
a9ea4c97-ef71-e140-e053-2995a90a97b6a9ea4c97-ef70-e140-e053-2995a90a97b62020-07-08Exact identifier
spl id: a9ea4c97-ef71-e140-e053-2995a90a97b6
spl set id: a9ea4c97-ef70-e140-e053-2995a90a97b6

Reported adverse events (FAERS/openFDA)#

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