FDA.reportPublic FDA data

POPPY AND IVY HAND SANITIZER

Manufacturer
Ester Co., Ltd.
Effective date
2020-11-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:40

Label at a glance#

ProductPOPPY AND IVY HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

Uses: For handwashing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Directions: Wet hands thoroughly with product Briskly rub hands together until dry Supervise children under 6 years in the use of this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ALCOHOL 70%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Glycerin, Carbomer, Tetrahydroxypropyl Ethylenediamine, Fragrance, Sodium Hyaluronate, 1,2-Hexanediol, Aloe Arborescens Leaf Extract, Butylene Glycol, Camellia Sinensis Leaf Extract

PURPOSE

OTC - PURPOSE SECTION

Purpose: ANTISEPTIC

WARNINGS

WARNINGS SECTION

Warnings:

For external use only.


Flammable. Keep away from heat or flame.


Do not use • in children less than 2 months of age • on open skin wounds


When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and consult a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep our of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

Uses:

For handwashing to decrease bacteria on the skin

Recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

Wet hands thoroughly with product

Briskly rub hands together until dry

Supervise children under 6 years in the use of this product

Other Information

OTHER SAFETY INFORMATION

Other Information:
Store at 15-30 °C (59-86 °F)
Avoid freezing and excessive heat above 40 °C (104 °F)

PACKAGE LABEL - POPPY & IVY HAND SANITIZER 2 mL Pouch

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of pouchImage of pouch

PACKAGE LABEL - POPPY & IVY HAND SANITIZER 60mL Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tubeImage of tube

PACKAGE LABEL - POPPY & IVY HAND SANITIZER 300mL Bottle

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

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
74004-020-012022-01-28C16284748780-1d6a99b39-990b-a426-e053-dadaa90af4c2e3c76b62-f914-4201-94c3-9f37083b971a
74004-020-022022-01-28C16284748780-1d6a99b39-990b-a426-e053-dadaa90af4c2e3c76b62-f914-4201-94c3-9f37083b971a
74004-020-032022-01-28C16284748780-1d6a99b39-990b-a426-e053-dadaa90af4c2e3c76b62-f914-4201-94c3-9f37083b971a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74004-020-01POPPY AND IVY HAND SANITIZER2 mL in 1 POUCHGEL22
74004-020-02POPPY AND IVY HAND SANITIZER60 mL in 1 TUBEGEL602
74004-020-03POPPY AND IVY HAND SANITIZER300 mL in 1 BOTTLE, PUMPGEL3002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74004-020POPPY AND IVY HAND SANITIZER (ALCOHOL) GEL [ESTER CO., LTD.]2Legacy NDC, 3 package rows20201114_e3c76b62-f914-4201-94c3-9f37083b971a.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
74004-02074004-020-01, 74004-020-02, 74004-020-03

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
EDETOLQ4R969U9FRIACT
HYALURONATE SODIUMYSE9PPT4THIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALOE ARBORESCENS LEAF09TD8L5SQVIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
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
b3e0d08a-8e02-051e-e053-2a95a90acdeee3c76b62-f914-4201-94c3-9f37083b971a2020-11-11WarningsExact identifier
spl id: b3e0d08a-8e02-051e-e053-2a95a90acdee
spl set id: e3c76b62-f914-4201-94c3-9f37083b971a

Reported adverse events (FAERS/openFDA)#

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