FDA.reportPublic FDA data

Goodwill Labs Advanced Hand Sanitizer

Manufacturer
Goodwill Brands, LLC
Effective date
2020-09-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:15:02

Label at a glance#

ProductGoodwill Labs Advanced Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

Place enough product in your palm to thoroughly cover your hands  Rub hands together until dry Recommended for repeated use Children under 6 years should be supervised when using this product

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

EHTYLALCOHOL, 62% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from sources of heat, fire or flame.

For external use only.

When using this product,

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops 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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to thoroughly cover your hands 
  • Rub hands together until dry
  • Recommended for repeated use
  • Children under 6 years should be supervised when using this product

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Aminomethyl Propanol, Carbomer, Methyl Gluceth-20

Other Information

SPL UNCLASSIFIED SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78700-00278700-002-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
METHYL GLUCETH-20J3QD0LD11PIACT
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
eb7d4428-24a4-b5e8-e053-2a95a90a48c6acda90bc-a0ad-7b84-e053-2995a90a88c22022-10-20WarningsExact identifier
spl set id: acda90bc-a0ad-7b84-e053-2995a90a88c2

Reported adverse events (FAERS/openFDA)#

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