Clean Supply

Manufacturer
Environmental Applied Technology Corporation
Effective date
2022-07-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:56:13

Label at a glance#

ProductClean Supply
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Put enough product inthe palm to cover your hand and rub hands together briskly until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F). May discolor certain fabricsor surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • 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.
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 immediately at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put enough product inthe palm to cover your hand and rub hands together briskly until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F).
  • May discolor certain fabricsor surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Acrylates Copolymer, Propylene Glycol, Trolamine, Tocopheryl Acetate, Deionized Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80366-002-012024-01-30C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-022024-01-30C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-032024-01-30C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-042024-01-30C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-052024-01-30C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-062024-01-30C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-012023-12-19C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-022023-12-19C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-032023-12-19C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-042023-12-19C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-052023-12-19C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-062023-12-19C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-012023-07-28C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-022023-07-28C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-032023-07-28C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-042023-07-28C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-052023-07-28C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce
80366-002-062023-07-28C16284748780-10191ceaa-668f-198a-e063-dbdaa90aec3ec02f480a-d41b-4a99-ac9a-ef216dd15cce

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80366-00280366-002-01, 80366-002-02, 80366-002-03, 80366-002-04, 80366-002-05, 80366-002-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
e4cf43dc-e873-8824-e053-2a95a90a452dc02f480a-d41b-4a99-ac9a-ef216dd15cce2022-07-27WarningsExact identifier
spl id: e4cf43dc-e873-8824-e053-2a95a90a452d
spl set id: c02f480a-d41b-4a99-ac9a-ef216dd15cce

Reported adverse events (FAERS/openFDA)#

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