HAND SANITIZER

Manufacturer
EXPORTADORA IN & OUT S DE RL DE CV
Effective date
2020-05-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:27

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure11 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

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

Antiseptic

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

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), Isopropyl alcohol, Ozonized vegetable glycerin and carboxymethul cellulose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label 1000 mllabel 1000 ml70% alcohol

Maximun moisturizing formula

Hand sanitizer

kills 99.9% of germs

topical, non steril solution

33.81fl oz/ 1000 ml

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
77210-0003-12022-01-28C16284748780-1d6a99b39-f2c4-a426-e053-dadaa90af4c2a5dd2c07-0eea-c5cf-e053-2a95a90ab7fa

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77210-0003-1HAND SANITIZER1000 mL in 1 BOTTLE, PLASTICGEL10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77210-0003HAND SANITIZER (ALCOHOL) GEL [EXPORTADORA IN & OUT S DE RL DE CV]1Legacy NDC, 1 package rows20200518_a5dd2c07-0eea-c5cf-e053-2a95a90ab7fa.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
77210-000377210-0003-1

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 · Source PDF

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
a5dd2c07-0eeb-c5cf-e053-2a95a90ab7faa5dd2c07-0eea-c5cf-e053-2a95a90ab7fa2020-05-17WarningsExact identifier
spl id: a5dd2c07-0eeb-c5cf-e053-2a95a90ab7fa
spl set id: a5dd2c07-0eea-c5cf-e053-2a95a90ab7fa

Reported adverse events (FAERS/openFDA)#

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