FDA.reportPublic FDA data

Antibacterial Wipes

Manufacturer
SJ Creations, Inc. | Tonic Bath & Body Products Shenzhen Ltd
Effective date
2021-09-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:36:24

Label at a glance#

ProductAntibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under 6 years of age should be supervised with using this product.

Storage and handling

Store between 20C to 25C (68F to 77F) May discolor some fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% v/v

Purpose

OTC - PURPOSE SECTION

Antibacterial, Wipe

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable.

Keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of contact, rince eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop.

Keep out of Reach of Children

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under 6 years of age should be supervised with using this product.

Other information

STORAGE AND HANDLING SECTION

  • Store between 20C to 25C (68F to 77F)
  • May discolor some fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Ethyl Alcohol, Glycerin, Propylene Glycol, Lavender Oil, Phenoxyethanol, Didecyldimethylammonium Chloride, Exylhexylglycerin, Fragrance (Parfum).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20124320124360ct NDC:43269-985-60

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43269-98543269-985-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
WATER059QF0KO0RIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
LAVENDER OILZBP1YXW0H8IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
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
cbe66131-331c-0abf-e053-2a95a90a86f0ae4e9fa0-40ab-b71c-e053-2995a90a0ff22021-09-13WarningsExact identifier
spl id: cbe66131-331c-0abf-e053-2a95a90a86f0
spl set id: ae4e9fa0-40ab-b71c-e053-2995a90a0ff2

Reported adverse events (FAERS/openFDA)#

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