FDA.reportPublic FDA data

Active Guard Foaming Hand Sanitizer

Manufacturer
HOME & BODY COMPANY
Effective date
2022-01-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:10:48

Label at a glance#

ProductActive Guard Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Place enough product in your palm to throughly cover hands Rub hands together briskly until dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride  0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

When using this product do not use in or near the eyes.
In case of contact, rinse eyes throughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product in your palm to throughly cover hands
  • Rub hands together briskly until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Fragrance, Glycerin, Isopropyl Alcohol, Polysorbate 20, Water (Aqua)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73746-001-012022-01-31C16284748780-1d6a99b39-873e-a426-e053-dadaa90af4c2Active Guard Foaming Hand Sanitizer
73746-001-012022-01-28C16284748780-1d6a99b39-873e-a426-e053-dadaa90af4c2Active Guard Foaming Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73746-00173746-001-01

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
ISOPROPYL ALCOHOLND2M416302IACT
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ea531ea0-29b8-161e-e053-2995a90a08bbcfd7db1a-35b0-427a-bffd-faab483f58b12022-10-05WarningsExact identifier
spl set id: cfd7db1a-35b0-427a-bffd-faab483f58b1

Reported adverse events (FAERS/openFDA)#

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