ECOFREAKS HAND SANITIZER

Manufacturer
Sanitizer Supply, LLC
Effective date
2020-12-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:02:27

Label at a glance#

ProductECOFREAKS HAND SANITIZER
Active ingredientALCOHOL
Label structure12 sections

Storage and handling

Other information 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

   Active ingredient                              Purpose

Ethyl Alcohol 80% v/v ......................... Antiseptic

OTC - PURPOSE SECTION

Purpose:  Antiseptic

WARNINGS SECTION

Warnings

For external use only.  Flammable.  Keep away from heat or flame.

INDICATIONS & USAGE SECTION

Uses

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

OTC - DO NOT USE SECTION

Do not use

  • on children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth.  In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.  These may be signs of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Place enough product on hands to cover all surfaces.  Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

STORAGE AND HANDLING SECTION

Otherinformation

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

INACTIVE INGREDIENT SECTION

Inactive ingredients  water, poly acrylic acid, aloe vera leaf, hydrogen peroxide, Mentha Piperita (Peppermint) Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90026-01290026-012-06, 90026-012-12, 90026-012-16, 90026-012-01, 90026-012-03, 90026-012-08, 90026-012-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
ddb9bd6b-c828-7d2d-e053-2995a90aa1154d6b6e43-d24b-4ded-8157-2cb5a6fb43732022-04-28WarningsExact identifier
spl set id: 4d6b6e43-d24b-4ded-8157-2cb5a6fb4373

Reported adverse events (FAERS/openFDA)#

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