Ritual Antiseptic Hand Sanitizer

Manufacturer
Shenzhen Derun'en Science & Technology Development Co., Ltd
Effective date
2020-12-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:59:59

Label at a glance#

ProductRitual Antiseptic Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Put proper amount of the hand sanitizer into your palm and gently rub it over your palms, the back of your hands, fingers and the spaces between your fingers. Rub your hands together continuously until they are dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Chloure de Benzalkonium 0.13% / Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Put proper amount of the hand sanitizer into your palm and gently rub it over your palms, the back of your hands, fingers and the spaces between your fingers. Rub your hands together continuously until they are dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water

Other information

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Importer info -

117725 Canada Inc

5778 boul Thimens, Ville St. Laurent , QC, Canada H4R 2K9

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10ML IN 1 BOTTLE NDC:55029-004-01

Label-10mlLabel-10ml

20ML IN 1 BOTTLE NDC:55029-004-02

Label-20mlLabel-20ml

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55029-00455029-004-01, 55029-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
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
b745bcec-7430-556b-e053-2995a90a8086b745b4d5-87bb-6ba2-e053-2a95a90aba9e2020-12-25WarningsExact identifier
spl id: b745bcec-7430-556b-e053-2995a90a8086
spl set id: b745b4d5-87bb-6ba2-e053-2a95a90aba9e

Reported adverse events (FAERS/openFDA)#

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