FDA.reportPublic FDA data

Healthy Hands Foaming Hand Sanitizer

Manufacturer
Morgan Gallacher Inc.
Effective date
2019-12-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:48:15

Label at a glance#

ProductHealthy Hands Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Uses For hand sanitizing to decrease bacteria on the skin

Dosage and administration

Directions Apply to hands. Work into a lather and let dry.  Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride...........................0.1 %

Uses

DOSAGE & ADMINISTRATION SECTION

Uses

  • For hand sanitizing to decrease bacteria on the skin

Purpose

OTC - PURPOSE SECTION

Purpose

Antimicrobial

Warnings

WARNINGS SECTION

Warnings

  • For external use only
  • When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not ingest.
  • Stop use and ask a doctor if irritation and redness develop and conditions persist.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical attention or contact a Poison Conrol Center immediately.

Directions

INDICATIONS & USAGE SECTION

Directions

  • Apply to hands. Work into a lather and let dry. 
  • Children under 6 years of age should be supervised when using this product.

Inert Ingredients:

INACTIVE INGREDIENT SECTION

Inactive Ingredients

  • water
  • cetrimonium chloride
  • laurtrimonium chloride
  • dihydroxyethyl cocamine oxide
  • glycereth-17 cocoate
  • citric acid 

Healthy Hands Foaming Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Healthy Hands Foaming Hand Sanitizerimage descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50241-98550241-985-01, 50241-985-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
water059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
aa750a9a-7425-ed4d-e053-2a95a90a1eaf127f56d7-ecbb-49ea-bfb2-c93c900d77462020-07-15WarningsExact identifier
spl set id: 127f56d7-ecbb-49ea-bfb2-c93c900d7746

Reported adverse events (FAERS/openFDA)#

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