PFA STRONGHOLD HAND SANITIZER

Manufacturer
STRONGHOLD TRADING LLC
Effective date
2021-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:54

Label at a glance#

ProductPFA STRONGHOLD HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Put enough product in the palm to cover hands & rub together briskly the liquid is dry. Children under 6 should be supervised when using Sanitizers.

Storage and handling

Store below 110°F (43°C) May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.066%

Purpose

OTC - PURPOSE SECTION

Disinfectant

Use

DOSAGE & ADMINISTRATION SECTION

Hand sanitizing to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product, avoid contact with the eyes.

In case of contact, flush eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develops and persists.

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

INDICATIONS & USAGE SECTION

  • Put enough product in the palm to cover hands & rub together briskly the liquid is dry.
  • Children under 6 should be supervised when using Sanitizers.

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine, Mentha Piperita (Peppermint) Oil, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Morus Alba Bark Extract, Panthenol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2565263benzalkonium chloride 0.066 % Topical GelPSN1
2565263benzalkonium chloride 0.00066 MG/MG Topical GelSCD1
2565263benzalkonium chloride 0.066 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80969-001-012023-01-30C16284748780-1f386c649-d290-0266-e053-dadaa90a7c1a80969-001-01 PFA HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80969-001-01PFA STRONGHOLD HAND SANITIZER60 mL in 1 BOTTLEGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80969-001PFA STRONGHOLD HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [STRONGHOLD TRADING LLC]1Legacy NDC, 1 package rows20210814_8af4767a-48d9-4c30-a0b9-baafcd19474e.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80969-00180969-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
c9797566-e51b-8f5f-e053-2a95a90ae74b8af4767a-48d9-4c30-a0b9-baafcd19474e2021-08-13WarningsExact identifier
spl id: c9797566-e51b-8f5f-e053-2a95a90ae74b
spl set id: 8af4767a-48d9-4c30-a0b9-baafcd19474e

Reported adverse events (FAERS/openFDA)#

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