FDA.reportPublic FDA data

XTRA

Manufacturer
Zhejiang Jifu Daily Chemical Co., Ltd.
Effective date
2025-03-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:56:47

Label at a glance#

ProductXTRA
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

for handwashing, to reduce bacteria on skin

Dosage and administration

Spray to wet hand. Scrub and rinse thoroughly.

Storage and handling

Store in a cool and dry pleace, and avoid direct sunlight.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for handwashing, to reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Do not use

OTC - DO NOT USE SECTION

Do not use with chlorine bleach to avoid irritating fumes.

Avoid contact with eyes.

OTC - WHEN USING SECTION

If eye contact occures fush thoroughly with water.

Do not ingest

OTC - ASK DOCTOR/PHARMACIST SECTION

Do not ingest. If ingested, drink plenty of water, contact a physician.

STORAGE AND HANDLING SECTION

Store in a cool and dry pleace, and avoid direct sunlight.

Directions

DOSAGE & ADMINISTRATION SECTION

Spray to wet hand. Scrub and rinse thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua）

Sodium Laureth Sulfate

Decyl Glucoside

Citric Acid

Methylisothiazlione

Phenoxyethanol

Sodium Benzoate

Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84987-001-01XTRA399 mL in 1 BOTTLE, SPRAYSPRAY3992

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84987-001XTRA (BENZALKONIUM CHLORIDE) SPRAY [ZHEJIANG JIFU DAILY CHEMICAL CO., LTD.]2Current NDC, 1 package rows20250309_27df3fce-3958-d4ea-e063-6394a90a1785.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84987-00184987-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM LAURETH SULFATEBPV390UAP0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
CITRIC ACID2968PHW8QPIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
XTRABENZALKONIUM CHLORIDEZhejiang Jifu Daily Chemical Co., Ltd.27df3fce-3958-d4ea-e063-6394a90a17852025-03-06WarningsExact identifier
ndc (package): 84987-001-01
ndc (product): 84987-001
ndc11 (package): 84987000101
spl id: 2fb7059d-5d89-3836-e063-6394a90a976c
spl set id: 27df3fce-3958-d4ea-e063-6394a90a1785

Reported adverse events (FAERS/openFDA)#

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