FDA.reportPublic FDA data

POPPY and IVY HAND SANITIZER

Manufacturer
Ester Co., Ltd.
Effective date
2020-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:07:08

Label at a glance#

ProductPOPPY and IVY HAND SANITIZER
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0606

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
74004-147-202022-01-28C16284748780-1d6a99b39-558e-a426-e053-dadaa90af4c2[Ester Co., Ltd.-POPPY and IVY HAND SANITIZER] 40 ml X 20 : 74004-147-20

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74004-147-20POPPY and IVY HAND SANITIZER20 in 1 BOXGEL201
74004-147-20POPPY and IVY HAND SANITIZER40 mL in 1 POUCHGEL401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74004-147POPPY AND IVY HAND SANITIZER (ALCOHOL) GEL [ESTER CO., LTD.]1Legacy NDC, 2 package rows20200421_a3bc55b0-a77b-6cae-e053-2995a90a4c4d.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
74004-14774004-147-20

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
ALOE ARBORESCENS LEAF09TD8L5SQVIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
GLYCERINPDC6A3C0OXIACT
EDETOLQ4R969U9FRIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
HYALURONATE SODIUMYSE9PPT4THIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
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
a3bc644e-0aa0-f08d-e053-2995a90acd2da3bc55b0-a77b-6cae-e053-2995a90a4c4d2020-04-17Exact identifier
spl id: a3bc644e-0aa0-f08d-e053-2995a90acd2d
spl set id: a3bc55b0-a77b-6cae-e053-2995a90a4c4d

Reported adverse events (FAERS/openFDA)#

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