ManiPure Hand Sanitizer

Manufacturer
ECON TRADING LLC
Effective date
2020-06-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:44

Label at a glance#

ProductManiPure Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Dispense enough product into your palm to adequately cover your hands. Rub hands together vigorously until dry. Children under the age of 6 should be supervised when using this product..

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Drug Facts:

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol ----------------------------- 70% v/v.

Porpuse

OTC - PURPOSE SECTION

ANTIMICROBIAL

Use:

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can

cause disease. For use when soap and water are not - available.

Warnings:

WARNINGS SECTION

Flammable Keep away from fire or flame.

For external use only

When using this product - do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. DO NOT INGEST OR INHALE. In the case of ingestion or inhalation, call poison control Center

DO NOT USE:

OTC - DO NOT USE SECTION

- In children less than 2 months of age.

- On open skin wounds

Stop use and ask a doctor

OTC - ASK DOCTOR/PHARMACIST SECTION

- if irritation or rash occurs, appears and last.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions:

DOSAGE & ADMINISTRATION SECTION

Dispense enough product into your palm to adequately cover your hands. Rub hands together vigorously until dry. Children under the age of 6 should be supervised when using this product..

Other Information:

STORAGE AND HANDLING SECTION

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Inactive Ingridients:

INACTIVE INGREDIENT SECTION

Water, Carboxymethyl cellulose, T-butyl alcohol, Denatonium benzoate

Package.Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1982 ml label1982 ml labelDrug Facts
Ethyl alcohol ----------------- 70% v/v.
Purpose: ANTIMICROBIAL

Indications : Hand Sanitizer to help
reduce bacteria that potentially can
cause disease. For use when soap and
water are not - available.

Warnings: Flammable Keep away from
fire or flame.For external use only When
using this product do not use in or near
the eyes. In case of contact, rinse eyes
thoroughly with water. DO NOT INGEST
OR INHALE. In the case of ingestion or
inhalation, call poison control.
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 ask a doctor if irritation
or rash occurs. These may be signs of a
serious condition.

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

Directions: Dispense enough product into
your palm to adequately cover your hands
. Rub hands together vigorously until dry.
Children under the age of 6 should be
supervised when using this product.

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

Inactive Ingridients:
Water, Carboxymethyl cellulose,
T-butyl alcohol, Denatonium benzoate

Distributed by:
Econ Trading LLC,
Newark, NJ

1892.71 ml 64 FL OZ

lot# 042020-1 Exp 04/2023

1892.71 ml 64 FL OZ NDC: 79339-001-12

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79339-001-122022-01-28C16284748780-1d6a99b39-dcc9-a426-e053-dadaa90af4c2a9553012-a8fe-0857-e053-2a95a90aeeec

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79339-001-12ManiPure Hand Sanitizer1892 mL in 1 BOTTLELIQUID18921

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79339-001MANIPURE HAND SANITIZER LIQUID [ECON TRADING LLC]1Legacy NDC, 1 package rows20200701_a9553012-a8fe-0857-e053-2a95a90aeeec.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
79339-00179339-001-12

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
a9553012-a8ff-0857-e053-2a95a90aeeeca9553012-a8fe-0857-e053-2a95a90aeeec2020-06-30WarningsExact identifier
spl id: a9553012-a8ff-0857-e053-2a95a90aeeec
spl set id: a9553012-a8fe-0857-e053-2a95a90aeeec

Reported adverse events (FAERS/openFDA)#

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