FDA.reportPublic FDA data

Hand Sanitizer Frozen 6 pack

Manufacturer
Townley, Inc.
Effective date
2016-06-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:14

Label at a glance#

ProductHand Sanitizer Frozen 6 pack Frozen 6pack
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, triethanolamine, PEG-40 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

Frozen 6 pack

Cotton Candy Scentend Hand Sanitizer

Cherry Scentend Hand Sanitizer

Grape Scentend Hand Sanitizer

Bubble Gum Scentend Hand Sanitizer

Lemon Scentend Hand Sanitizer

Watermelon Scentend Hand Sanitizer

2 FL OZ (59mL)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58737-151-012021-01-29C16284748780-1ba0f9c33-4062-a910-e053-dadaa90a0b8534b54c47-6a32-65de-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58737-151-01Hand Sanitizer Frozen 6 packFrozen 6pack59 g in 1 BOTTLEGEL591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58737-151HAND SANITIZER FROZEN 6 PACK FROZEN 6PACK (BENZALKONIUM CHLORIDE) GEL [TOWNLEY, INC.]1Legacy NDC, 1 package rows20160607_34b54c47-6a32-65de-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58737-15158737-151-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM HYDROXIDE55X04QC32IIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
COCETH-7 CARBOXYLIC ACID35KO064932IACT
PPG-1 TRIDECETH-61K7417JX6QIACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)4Q93RCW27EIACT
TROLAMINE9O3K93S3TKIACT
PEG-40 CASTOR OIL4ERD2076EFIACT
PPG-1-PEG-9 LAURYL GLYCOL ETHER5R8J43K25LIACT
METHOXY PEG-406AXS45P1QUIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
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
34b54c47-6a33-65de-e054-00144ff8d46c34b54c47-6a32-65de-e054-00144ff8d46c2016-06-06WarningsExact identifier
spl id: 34b54c47-6a33-65de-e054-00144ff8d46c
spl set id: 34b54c47-6a32-65de-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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