FDA.reportPublic FDA data

Antibacterial wipes

Manufacturer
Yuhan Green Tech Co.
Effective date
2023-08-03
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 21:27:43

Label at a glance#

ProductAntibacterial wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

Direction

DOSAGE & ADMINISTRATION SECTION

Open the plastic lic. Peel back front label slowly

Do not use

OTC - DO NOT USE SECTION

do not flush

do not use if you are allergic to any of the ingredients

when using this product

OTC - WHEN USING SECTION

when using this product do not get into eyes.

if contact occurs, rinse thoroughly whit water.

Warnings

WARNINGS SECTION

for external sue only.

sotre away from direct sunlight or high temperature.

use caution near electric appliances to avoid electric shock.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Stop use and ask a doctor.

OTC - STOP USE SECTION

stop use and ask a doctor if irritationor or rash edvelopes and continues for more than 72 hours.

Use

INDICATIONS & USAGE SECTION

peel back front label slowy.

use caution near electric appliances to avoid electric shock

ask a doctor

OTC - ASK DOCTOR SECTION

If swallowed, get medical help or contact a Poison control center right away

Other information

OTHER SAFETY INFORMATION

7.9 in x 5.9 in (20cm x15cm )

INACTIVE INGREDIEINT

INACTIVE INGREDIENT SECTION

WATER
ORANGE OIL
PINUS DENSIFLORA LEAF

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

78583-302-01

78252-302-0178252-302-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78583-302-012023-08-03C16284748780-1f386c64a-107b-0266-e053-dadaa90a7c1a78583-302-01 sanitizer
78583-302-012023-01-30C16284748780-1f386c64a-107b-0266-e053-dadaa90a7c1a78583-302-01 sanitizer

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78583-30278583-302-01

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
ORANGE OILAKN3KSD11BIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PINUS DENSIFLORA LEAFQ1Q9P50WIYIACT

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
02101d4b-c625-d989-e063-6294a90a08aeaab19d8d-c80b-3bbf-e053-2995a90ad6ea2023-08-03WarningsExact identifier
spl id: 02101d4b-c625-d989-e063-6294a90a08ae
spl set id: aab19d8d-c80b-3bbf-e053-2995a90ad6ea

Reported adverse events (FAERS/openFDA)#

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