FDA.reportPublic FDA data

20CT MOUTAIN DEW HAND SANI WIPES

Manufacturer
Zhejiang Bright Care Co., Ltd
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-07-17 21:35:44

Label at a glance#

ProductMOUTAIN DEW HAND SANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 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 without wiping
  • Supervise children under 6 years 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.

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 Poison Control Center right away.

OTC - ASK DOCTOR SECTION

Stop use and ask doctor if irritation or redness develop 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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810187382628GTIN-13: 0810187382628
EAN-13: 0810187382628
GTIN-12: 810187382628
UPC-A: 810187382628
GTIN storage (14 digits): 00810187382628		54fca2ac-b251-1b4e-e063-6394a90a137c.jpg, wipe031.jpg

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
85844-50485844-504-01, 85844-504-02

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
AQUA059QF0KO0RIACT

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
MOUTAIN DEW HAND SANITIZING WIPESHAND SANITIZING WIPESZhejiang Bright Care Co., Ltd54fbbdde-ef7b-0a8b-e063-6294a90ad9e42026-06-24WarningsExact identifier
ndc (package): 85844-504-01
ndc (package): 85844-504-02
ndc (product): 85844-504
ndc11 (package): 85844050402
ndc11 (package): 85844050401
spl id: 54fbbde6-246c-21b0-e063-6394a90a28c0
spl set id: 54fbbdde-ef7b-0a8b-e063-6294a90ad9e4

Reported adverse events (FAERS/openFDA)#

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