FDA.reportPublic FDA data

PEPSI VANILLA HAND SANITIZER WIPES

Manufacturer
Zhejiang Bright Care Co., Ltd
Effective date
2026-06-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:35:36

Label at a glance#

ProductVANILL HAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin
  • Recommended for repeated use

OTC - WHEN USING SECTION

  • Rub wipe throughly over all surfaces of both hands.
  • Allow to dry wihtout wiping
  • Supervise chilfren under 6 yeras old
  • Not recommended for infants.
  • Dispose of wipe in trash.
  • Do not flush

DOSAGE & ADMINISTRATION SECTION

Wipe hands, skin surface thoroughly; allow to dry.

Use as needed for skin disinfection.

For external use only.

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.

WARNINGS SECTION

For external use only.

When using this product key away from eye

In case of eye contact,rinse eyes with doctor.

Stop use and ask a doctor if:

irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact Poison Control Centre right away

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if irritation or redessdevelop or lasts for more than 72 hours

INACTIVE INGREDIENT SECTION

Aqua,Phenoxyethano,Aloe Barbadensis Extrac,Parfum

OTC - QUESTIONS SECTION

Questions ? 212-689-6008

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85844-50085844-500-01, 85844-500-02

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
FRAGRANCE 135765EM498GW35IACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
AQUA059QF0KO0RIACT
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
VANILL HAND SANITIZING WIPESHAND SANITIZING WIPESZhejiang Bright Care Co., Ltd54e9d23b-45e5-5e53-e063-6394a90a60662026-06-23WarningsExact identifier
ndc (package): 85844-500-01
ndc (package): 85844-500-02
ndc (product): 85844-500
ndc11 (package): 85844050001
ndc11 (package): 85844050002
spl id: 54e9d23b-45e6-5e53-e063-6394a90a6066
spl set id: 54e9d23b-45e5-5e53-e063-6394a90a6066

Reported adverse events (FAERS/openFDA)#

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