FDA.reportPublic FDA data

NovaGel Alcohol-free Foaming Hand Sanitizer

Manufacturer
Zhejiang Hongshiliang Health Technology Co Ltd
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:19:02

Label at a glance#

ProductNovaGel Alcohol-free Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Benzalkonium chloride 0.1% Antimicrobial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on skin

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children- If swallowed, get medical help or contact a Poison Control Center right away.

Warning

WARNINGS SECTION

Warnings. For external use only.

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

Stope use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

INSTRUCTIONS FOR USE SECTION

Directions - Pump a small amount of foam onto palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients- water, glycerin, sodium lauryl sulfate, fragrance

Dosage and Adminstration Section

DOSAGE & ADMINISTRATION SECTION

Benzalkonium Chloride 0.1%

Directions - Pump a small amount of foam onto palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Purpose Section

OTC - PURPOSE SECTION

Purpose

Antimicrobial

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78360-001-012022-01-28C16284748780-1d6a99b39-5bc5-a426-e053-dadaa90af4c2a45c1ac2-a878-4b11-e053-2995a90a4798

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78360-001-01NovaGel Alcohol-free Foaming Hand Sanitizer59.15 g in 1 BOTTLE, PLASTICLIQUID59.151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78360-001NOVAGEL ALCOHOL-FREE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE HAND SANITIZER) LIQUID [ZHEJIANG HONGSHILIANG HEALTH TECHNOLOGY CO LTD]1Legacy NDC, 1 package rows20200626_a45c1ac2-a878-4b11-e053-2995a90a4798.zip

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
78360-00178360-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAURYL SULFATE368GB5141JIACT

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
a45c1ac2-a879-4b11-e053-2995a90a4798a45c1ac2-a878-4b11-e053-2995a90a47982020-04-28WarningsExact identifier
spl id: a45c1ac2-a879-4b11-e053-2995a90a4798
spl set id: a45c1ac2-a878-4b11-e053-2995a90a4798

Reported adverse events (FAERS/openFDA)#

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