HAND SANITIZER

Manufacturer
EXPORTADORA IN & OUT S DE RL DE CV
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:12

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

Hand sanitizer to derease virus and bacteria on the skin that could cause disease. For when water and soap are not available Recommended for repeated use

Dosage and administration

-Put enough product in your palm to cover hands and rub hands together briskly until dry without wiping -For Children under 6 years of age should be supervised when using hando3 -Not recommended for infants

Storage and handling

Sotre below 105 F (40C) May discolor certain fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alchol v/v - 70%

Purposes

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to derease virus and bacteria on the skin that could cause disease. For when water and soap are not available

Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame

When using this product

OTC - DO NOT USE SECTION

keep out eyes, ears and mouth. Do not use in or near the eyes.

In case of contact with eyes, flush thorougly with water

Avoid contact with broken skin

Do not inhale or ingest

When using this product

OTC - WHEN USING SECTION

Keep out of eyes, ears and mouth. Do not use in or near the eyes.

In case of contact eyes, flush thorougly with water

Avoid contact with broken skin

Do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation and redness develop

Conditions persists for more than 72 hours

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a posion control center right away

Directions

DOSAGE & ADMINISTRATION SECTION

-Put enough product in your palm to cover hands and rub hands together briskly until dry without wiping

-For Children under 6 years of age should be supervised when using hando3

-Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Sotre below 105 F (40C)

May discolor certain fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water (Aqua), vegetable glycerin and carboxymethul cellulose

for the 1,000 lt label

WARNINGS AND PRECAUTIONS SECTION

Firefighting CAUTION: all these products have a very low flash point: use water spray when fighting fire may be inefficient: CAUTION: Alcohol-resistant foam should be used.SMALL FIRE: Dry Chemicals, co2, water spray or alcohol-resistant foam. LARGE FIRE: Water spray, fog or alcohol resistant foam. Do not use straight streams. Move containers from fire area if you can do it without risk. FIRE INVOLVING TANKS OR CAR/TRAILERS LOADS: Fight fire for maximun distance or use unmanned hose holders or monito nozzles: Cool containers with flooding quiantities of water until well after fire is out. Withdraw immediatly in case of rising sounf from venting safety devices or discoloration of thank. ALWAYS stay away from tanks engulfed in fire. For massive fire, use unmaned hose holders or monitor nozzles; if this is imposible. Withdraw from area and let the fire burn.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 1000 ltLabel 1000 ltlabel 1ltlabel 1lthando3

hand sanitizer gel

antiviral & antibacterial ozonized gel

leaves hands soft

contains moisturizers

paraben free

phthalate free

formaldehyde donor free

33.8 fl oz (1 liter)

264.17 Gallons ( 1000 liters)

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
77210-0004-12022-01-28C16284748780-1d6a99b39-3e69-a426-e053-dadaa90af4c2a62d2015-4184-7ef6-e053-2a95a90ae23e
77210-0004-22022-01-28C16284748780-1d6a99b39-3e69-a426-e053-dadaa90af4c2a62d2015-4184-7ef6-e053-2a95a90ae23e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77210-0004-1HAND SANITIZER1000 mL in 1 BOTTLE, PLASTICGEL10001
77210-0004-2HAND SANITIZER1000000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKGEL10000001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77210-0004HAND SANITIZER (ALCOHOL) GEL [EXPORTADORA IN & OUT S DE RL DE CV]1Legacy NDC, 2 package rows20200522_a62d2015-4184-7ef6-e053-2a95a90ae23e.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77210-000477210-0004-1, 77210-0004-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a62d2015-4185-7ef6-e053-2a95a90ae23ea62d2015-4184-7ef6-e053-2a95a90ae23e2020-05-21WarningsExact identifier
spl id: a62d2015-4185-7ef6-e053-2a95a90ae23e
spl set id: a62d2015-4184-7ef6-e053-2a95a90ae23e

Reported adverse events (FAERS/openFDA)#

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