FDA.reportPublic FDA data

SANITIZING WIPES

Manufacturer
Jinhua Aidi Daily Chemical Co., Ltd.
Effective date
2024-01-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:13:48

Label at a glance#

ProductSANITIZING WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Tear open packet, remove wipe. Wet hands or surface thoroughly with product and let air dry. Throw used wipe in trash. Do not flush. Adults and children 2 years and over Apply to hands. Allow skin to dry without Wiping. Children under 2 years Ask a doctor before use.

Storage and handling

Store between 15-30C(59-86F) Avoid freezing and excessive heat above 40C(104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial Agent

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of the ingredients.

OTC - WHEN USING SECTION

When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear open packet, remove wipe.
  • Wet hands or surface thoroughly with product and let air dry.
  • Throw used wipe in trash. Do not flush.

Adults and children 2 years and over

  • Apply to hands.
  • Allow skin to dry without Wiping.

Children under 2 years

  • Ask a doctor before use.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C(59-86F)
  • Avoid freezing and excessive heat above 40C(104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Phenoxyethanol, Ethylhexylglycerin, DDAC, Propylene Glycol, Glycerin, Citrus extract, Purified Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 PATCH in 1 PACKET NDC: 75181-005-01 30PCS label30PCS label

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
75181-00575181-005-01

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
ETHYLHEXYLGLYCERIN147D247K3PIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRUS FRUITXDK00Z8012IACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
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
2a183444-5d5b-a867-e063-6294a90a3ce4aaa3e7bf-c1d2-5050-e053-2995a90a127e2024-12-25WarningsExact identifier
spl set id: aaa3e7bf-c1d2-5050-e053-2995a90a127e

Reported adverse events (FAERS/openFDA)#

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