FDA.reportPublic FDA data

ENVIRO E3 RATED SANITIZER

Manufacturer
IMPERIAL VALLEY DISTRIBUTING, INC | M CHEM S.A DE C.V.
Effective date
2020-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:37

Label at a glance#

ProductENVIRO E3 RATED SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeat use.

Dosage and administration

Place enough product in your palm to thoroughly cover your hands.  Rub hands together briskly until dry. No rinsing  required. No towels needed

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease.
  • Recommended for repeat use.

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.

Stop use and ask a doctor

- If irritation or rash appears and lasts.

Keep out of reach of children. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands. 
  • Rub hands together briskly until dry.
  • No rinsing  required.
  • No towels needed

Other information

SPL UNCLASSIFIED SECTION

   Do not store above 110⁰F(43⁰C).

- May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Triethanolamine, Acrylates/C10-C30 Alkyl Akrylate, Crosspolymer

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
74693-001-012022-01-28C16284748780-1d6a99b39-6f31-a426-e053-dadaa90af4c2ENVIRO E3 RATED sanitizer
74693-001-022022-01-28C16284748780-1d6a99b39-6f31-a426-e053-dadaa90af4c2ENVIRO E3 RATED sanitizer
74693-001-032022-01-28C16284748780-1d6a99b39-6f31-a426-e053-dadaa90af4c2ENVIRO E3 RATED sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74693-001-01ENVIRO E3 RATED SANITIZER800 mL in 1 BOTTLE, PLASTICLIQUID8001
74693-001-02ENVIRO E3 RATED SANITIZER1000000 mL in 1 BOTTLE, PLASTICLIQUID10000001
74693-001-03ENVIRO E3 RATED SANITIZER37854 mL in 1 BOTTLE, PLASTICLIQUID378541

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74693-001ENVIRO E3 RATED SANITIZER (ETHANOL ALCOHOL) LIQUID [IMPERIAL VALLEY DISTRIBUTING, INC]1Legacy NDC, 3 package rows20200410_901fdf5d-acfe-4ad0-9144-11244204dbf1.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74693-00174693-001-01, 74693-001-02, 74693-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT

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
a1b53627-2145-485c-baf8-b3e7eb060b04901fdf5d-acfe-4ad0-9144-11244204dbf12020-04-07WarningsExact identifier
spl id: a1b53627-2145-485c-baf8-b3e7eb060b04
spl set id: 901fdf5d-acfe-4ad0-9144-11244204dbf1

Reported adverse events (FAERS/openFDA)#

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