FDA.reportPublic FDA data

SouthPoint sanitizer wipe

Manufacturer
Shenzhen Lantern Science Co.,Ltd.
Effective date
2020-08-30
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:26:21

Label at a glance#

ProductSouthPoint sanitizer wipe 01
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

remove and unfold wipe wipe hands thoroughly and allow to dry do not flush

Label contents#

Full prescribing information#

drug facts

DESCRIPTION SECTION

SouthPoint sanitizer wipeSouthPoint sanitizer wipe

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient purpose

Benzalkonium Chloride 0.1% Antimicrobial

Use

OTC - PURPOSE SECTION

for hand sanitizing to decrease bacteria on skin

recommended for repeated use.

warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes.In case of eye contact,flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops,or if condition persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed,get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

remove and unfold wipe

wipe hands thoroughly and allow to dry

do not flush

Inactive ingredient

INACTIVE INGREDIENT SECTION

Aqua,phenoxyethanol,polysorbate 20,disodium EDTA,sodium citrate,fragrance.

usage

INDICATIONS & USAGE SECTION

Remove and unfold wipe

wipe hands thoroughly and allow to dry.

do not flush

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SouthPoint sanitizer wipeSouthPoint sanitizer wipe

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54860-327-012022-01-28C16284748780-1d6a99b39-ae79-a426-e053-dadaa90af4c2SouthPoint sanitizer wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54860-327-01SouthPoint sanitizer wipe011 in 1 PACKETCLOTH18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54860-327SOUTHPOINT SANITIZER WIPE 01 (BENZALKONIUM CHLORIDE) CLOTH [SHENZHEN LANTERN SCIENCE CO.,LTD.]8Legacy NDC, 1 package rows20200831_ae23ac83-ff9f-50e5-e053-2995a90aceb4.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
54860-32754860-327-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEACH3OKE88I3QGIACT
SODIUM CITRATE1Q73Q2JULRIACT
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ae23a069-d01c-0b46-e053-2a95a90a3414ae23ac83-ff9f-50e5-e053-2995a90aceb42020-08-30WarningsExact identifier
spl id: ae23a069-d01c-0b46-e053-2a95a90a3414
spl set id: ae23ac83-ff9f-50e5-e053-2995a90aceb4

Reported adverse events (FAERS/openFDA)#

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