FDA.reportPublic FDA data

FVJIA disinfectant

Manufacturer
Hunan Fujia Environmental Safety Technology Co., Ltd
Effective date
2022-05-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:49:37

Label at a glance#

ProductFVJIA disinfectant
Active ingredientBENZALKONIUM CHLORIDE, DIDECYLDIMONIUM CHLORIDE
Label structure13 sections

Dosage and administration

Spray on the surface of the skin and let it dry naturally

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

FVJIA disinfectant

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Didecyl Dimethyl Ammonium Chloride 0.60g/100mL

Benzalkonium chloride 0.20g/100mL

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

FVJIA disinfectant to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray on the surface of the skin and let it dry naturally

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Polyhexamethylene biguanide hydrochloride
Distilled water
Glutaric dialdehyde

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

112233

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82170-101-012023-07-28C16284748780-10191ceaa-6208-198a-e063-dbdaa90aec3ec9d776a3-2906-3f13-e053-2995a90ae9e3
82170-101-022023-07-28C16284748780-10191ceaa-6208-198a-e063-dbdaa90aec3ec9d776a3-2906-3f13-e053-2995a90ae9e3
82170-101-032023-07-28C16284748780-10191ceaa-6208-198a-e063-dbdaa90aec3ec9d776a3-2906-3f13-e053-2995a90ae9e3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82170-101-01FVJIA disinfectant50 mL in 1 BOTTLESPRAY503
82170-101-02FVJIA disinfectant100 mL in 1 BOTTLESPRAY1003
82170-101-03FVJIA disinfectant240 mL in 1 BOTTLESPRAY2403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82170-101FVJIA DISINFECTANT (DIDECYL DIMETHYL AMMONIUM CHLORIDE, BENZALKONIUM CHLORIDE) SPRAY [HUNAN FUJIA ENVIRONMENTAL SAFETY TECHNOLOGY CO., LTD]3Legacy NDC, 3 package rows20220519_c9d776a3-2906-3f13-e053-2995a90ae9e3.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82170-10182170-101-01, 82170-101-02, 82170-101-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
POLIHEXANIDE HYDROCHLORIDE4XI6112496IACT
GLUTARALDEHYDET3C89M417NIACT
WATER059QF0KO0RIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BACTIB

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
df4506e5-014e-6753-e053-2995a90a37c6c9d776a3-2906-3f13-e053-2995a90ae9e32022-05-18WarningsExact identifier
spl id: df4506e5-014e-6753-e053-2995a90a37c6
spl set id: c9d776a3-2906-3f13-e053-2995a90ae9e3

Reported adverse events (FAERS/openFDA)#

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