Meni Hand Sanitizer Gel

Manufacturer
Seekr Global Inc. | Corporativo Cubrete, S.A. de C.V.
Effective date
2020-07-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:23:13

Label at a glance#

ProductMeni Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping, For children under 6, use only under adult supervision. 

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

OTC - PURPOSE SECTION

(Hand Antiseptic)

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Carbomer, Triethanolamine.

Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping, For children under 6, use only under adult supervision. 

Use:

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

Warnings:

WARNINGS SECTION

For external use only.

Flammable - keep away from fire or flames.

Keep ouit of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Do not use

OTC - DO NOT USE SECTION

in eyes, In case of contact, rinse thoroughly with water.

Stop use and consult a doctor if

OTC - STOP USE SECTION

irritation or redness develops and persist for more for more than 72 hours.

SPL UNCLASSIFIED SECTION

Store at 20C to 25C (68F to 77F), may discolor certain fabrics.

Package Labeling:125 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:500 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:1000 mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79439-000-002022-01-28C16284748780-1d6a99b39-441a-a426-e053-dadaa90af4c2Meni Hand Sanitizer Gel
79439-000-012022-01-28C16284748780-1d6a99b39-441a-a426-e053-dadaa90af4c2Meni Hand Sanitizer Gel
79439-000-022022-01-28C16284748780-1d6a99b39-441a-a426-e053-dadaa90af4c2Meni Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79439-000-00Meni Hand Sanitizer125 mL in 1 BOTTLEGEL1253
79439-000-01Meni Hand Sanitizer500 mL in 1 BOTTLEGEL5003
79439-000-02Meni Hand Sanitizer1000 mL in 1 BOTTLEGEL10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79439-000MENI HAND SANITIZER (ALCOHOL) GEL [SEEKR GLOBAL INC.]3Legacy NDC, 3 package rows20200731_99b14b22-9ee9-4f6d-ab6e-bcb57120aa01.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79439-00079439-000-00, 79439-000-01, 79439-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
aba9c07e-0a45-9b74-e053-2a95a90a2d9199b14b22-9ee9-4f6d-ab6e-bcb57120aa012020-07-30WarningsExact identifier
spl id: aba9c07e-0a45-9b74-e053-2a95a90a2d91
spl set id: 99b14b22-9ee9-4f6d-ab6e-bcb57120aa01

Reported adverse events (FAERS/openFDA)#

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