Hand Sanitizer

Manufacturer
DGH Pharma, Inc.
Effective date
2020-10-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:31:21

Label at a glance#

ProductHand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Rub thoroughly over all surfaces of both hands. Rub hands toghether briskly unitl dry.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.10% w/w. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

To eliminate viruses and bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub thoroughly over all surfaces of both hands.
  • Rub hands toghether briskly unitl dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Citrus Sinensis (Orange) Fruit Oil, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerin, Hydroxyethylcellulose, PEG-8, PEG-90, Potassium Sorbate, Polysorbate 20, Purified Water, Quercus Borealis Bark Extract

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118 mL Sanitizer Label118 mL Sanitizer Label

Impact Diversity Solutions Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

118 mL Impact Sanitizer118 mL Impact Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049228benzalkonium chloride 0.1 % Topical GelPSN2
1049228benzalkonium chloride 0.001 MG/MG Topical GelSCD2
1049228benzalkonium chloride 0.1 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77238-221-142022-01-28C16284748780-1d6a99b39-cb42-a426-e053-dadaa90af4c2Hand Sanitizer
77238-221-242022-01-28C16284748780-1d6a99b39-cb42-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77238-221-14Hand Sanitizer118 mL in 1 BOTTLEGEL1182
77238-221-24Hand Sanitizer118 mL in 1 BOTTLEGEL1182

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77238-221HAND SANITIZER (BENZALKONIUM CHLORIDE) GEL [DGH PHARMA, INC.]2Legacy NDC, 2 package rows20201010_a878c2af-ca19-56f9-e053-2a95a90a40e3.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77238-22177238-221-14, 77238-221-24

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
b1445906-4c43-9887-e053-2995a90a6f82a878c2af-ca19-56f9-e053-2a95a90a40e32020-10-09WarningsExact identifier
spl id: b1445906-4c43-9887-e053-2995a90a6f82
spl set id: a878c2af-ca19-56f9-e053-2a95a90a40e3

Reported adverse events (FAERS/openFDA)#

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