EcoFreaks Foaming Hand Sanitizer Peppermint

Manufacturer
Sanitizer Supply, LLC
Effective date
2020-12-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:02:07

Label at a glance#

ProductEcoFreaks Foaming Hand Sanitizer Peppermint
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#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                              Purpose

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

OTC - PURPOSE SECTION

Purpose   Antiseptic

INDICATIONS & USAGE SECTION

Use[s]

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

WARNINGS SECTION

Warnings

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

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 dontact with eyes, rinase 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

Other information

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

INACTIVE INGREDIENT SECTION

Inactive ingredients  purified water, aloe vera leaf, PEG-10 Dimethicone, 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
90026-02290026-022-16, 90026-022-90

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
ddb98b05-323f-9a30-e053-2a95a90a2dc214767fa5-74ce-4b4f-93cd-a6759d18d2c72022-04-28WarningsExact identifier
spl set id: 14767fa5-74ce-4b4f-93cd-a6759d18d2c7

Reported adverse events (FAERS/openFDA)#

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