Avengers Marvel Hand Sanitizer

Manufacturer
Townley, Inc.
Effective date
2016-08-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:45

Label at a glance#

ProductAvengers Marvel Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose: Antibacterial

OTC - PURPOSE SECTION

Use

To decrease bacteria on the skin that could cause disease.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Warnings

  • for external use only-hands.
  • keep out of eyes. avoid contact with broken skin.
  • stop use and ask a Doctor if irritation or redness develops.
  • do not inhale or ingest. if swallowed, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Rub a dime sized drop into hands.
  • For children under 6 use under adult supervision.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

water (aqua/eau), glycerin, coceth-7, PPG-1-PEG-9 lauryl glycol ether, carbomer, hydrogenated castor oil, fragrance (parfum).

May Contain

Red 40 (CI 16035), Red 33 (CI 17200), Blue 1 (CI 42090), Yellow 5 (CI 19140).

INDICATIONS & USAGE SECTION

Avengers Marvel Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58737-162-012021-01-29C16284748780-1ba0f9c33-4acc-a910-e053-dadaa90a0b8539bbf572-e889-2c74-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58737-162-01Avengers Marvel Hand Sanitizer59 g in 1 BOTTLEGEL591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58737-162AVENGERS MARVEL HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [TOWNLEY, INC.]1Legacy NDC, 1 package rows20160810_39bbf572-e889-2c74-e054-00144ff8d46c.zip

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
58737-16258737-162-01

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
39bc30d5-f93f-696e-e054-00144ff88e8839bbf572-e889-2c74-e054-00144ff8d46c2016-08-10WarningsExact identifier
spl id: 39bc30d5-f93f-696e-e054-00144ff88e88
spl set id: 39bbf572-e889-2c74-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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