MODAKA

Manufacturer
WE LABS COMPANY LIMITED
Effective date
2020-05-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:27

Label at a glance#

ProductMODAKA ALCOHOL HAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

Active Ingredient (s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Anti-Bacterial, Anti-microbial and Germs

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Flammable, keep away from fire and flames

For external use only

When using this product

- do not get into eyes

- if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

- irritation and redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Direction No water required. Apply to hands, rub in, ensuring contact with fingernails and in between fingers. Can also be applied to the body.

INACTIVE INGREDIENT SECTION

Inactive Ingredients water, Propylene Glycol, Trehalose, Sodium Benzoate, Potasssium Sorbate, Dendrobium Bigibbum (Orchid) Flower Extract, Calendula Officinalis (Marigold) Flower Extract, Fragrance, Allantoin.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77779-001-012022-01-28C16284748780-1d6a99b39-dacb-a426-e053-dadaa90af4c2modaka alcohol hand sanitizer
77779-001-022022-01-28C16284748780-1d6a99b39-dacb-a426-e053-dadaa90af4c2modaka alcohol hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77779-001-01MODAKAALCOHOL HAND SANITIZER60 mL in 1 BOTTLE, SPRAYLIQUID601
77779-001-02MODAKAALCOHOL HAND SANITIZER1000 mL in 1 BOTTLE, PLASTICLIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77779-001MODAKA ALCOHOL HAND SANITIZER (ETHYL ALCOHOL) LIQUID [WE LABS COMPANY LIMITED]1Legacy NDC, 2 package rows20200601_856eb26c-adea-4a58-a100-3b6e06d58ed4.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
77779-00177779-001-01, 77779-001-02

Ingredients#

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

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

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
6aa9e795-bfd3-45f8-9de7-8d7dc8fa326e856eb26c-adea-4a58-a100-3b6e06d58ed42020-05-15WarningsExact identifier
spl id: 6aa9e795-bfd3-45f8-9de7-8d7dc8fa326e
spl set id: 856eb26c-adea-4a58-a100-3b6e06d58ed4

Reported adverse events (FAERS/openFDA)#

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