FDA.reportPublic FDA data

ECOssential Personal PPE Kit

Manufacturer
Hunter Amenities International Limited
Effective date
2022-01-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:11:25

Label at a glance#

ProductECOssential Personal PPE Kit
Active ingredientALCOHOL
Label structure16 sections

Indications and uses

Antiseptic (skin) cleanser Medicated (skin) cleanser Antibacterial (skin) cleanser Kills harmful bacteria/germs Effective in destroying (harmful) bacteria to provide antiseptic cleansing For personal hand hygiene to help prevent the spread of bacteria

Dosage and administration

Adults and children over 2 years. For occasional and personal domestic use. Supervise children when they use this product. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Label contents#

Full prescribing information#

Active Ingredient (v/v)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0 %

Purpose

OTC - PURPOSE SECTION

Antiseptic skin cleanser

Uses

INDICATIONS & USAGE SECTION

  • Antiseptic (skin) cleanser
  • Medicated (skin) cleanser
  • Antibacterial (skin) cleanser
  • Kills harmful bacteria/germs
  • Effective in destroying (harmful) bacteria to provide antiseptic cleansing
  • For personal hand hygiene to help prevent the spread of bacteria

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if

OTC - STOP USE SECTION

irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Flammability warnings. Keep away from open flame and sources of heat.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 2 years.

  • For occasional and personal domestic use.
  • Supervise children when they use this product.
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua/Water/Eau, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine,parfum (Fragrance), Aloe Barbadensis Leaf extract,Avena Sativa Kernal Extract, PEG-40 Hydrogenated Castor Oil, Tocopherol Acetate.

Questions?

OTC - QUESTIONS SECTION

1-800-668-1483

Active ingredient (v/v)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0 %

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Sanitizing wipes to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear open, unfold, and apply to hands
  • Children under 6 years of age should be supervised when using this product

Other information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin

Questions?

OTC - QUESTIONS SECTION

1-800-668-1483

Package Labeling:Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KitKit

Package Labeling:30ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:Wipe

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65910-01965910-019-01
65910-02065910-020-01
65910-02165910-021-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
TROLAMINE9O3K93S3TKIACT
ALOE VERA LEAFZY81Z83H0XIACT
OATZ6J799EAJKIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MACTIB

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
e88196ce-0690-0ce8-e053-2995a90a0bf5b0656526-8606-31bb-e053-2a95a90afb1c2022-09-12WarningsExact identifier
spl set id: b0656526-8606-31bb-e053-2a95a90afb1c

Reported adverse events (FAERS/openFDA)#

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