FDA.reportPublic FDA data

Ritual Antiseptic Hand Sanitizer

Manufacturer
Shenzhen Derun'en Science & Technology Development Co., Ltd
Effective date
2021-01-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:13

Label at a glance#

ProductRitual Antiseptic Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Do not use in the eyes

Stop use and ask a doctor if

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep out of reach of childen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized water

Other information

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Importer info:

Essence 360

5778 Boulevard Thimens, Saint-Laurent, QC, H4R 2K9, Canada

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10ML IN 1 BOTTLE NDC:55029-005-01

Label-10mlLabel-10ml

20ML IN 1 BOTTLE NDC:55029-005-02

Label-20mlLabel-20ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55029-005-012022-07-29C16284748780-1e4f33bdf-a101-d8a0-e053-dadaa90a6e4eRitual Antiseptic Hand Sanitizer
55029-005-022022-07-29C16284748780-1e4f33bdf-a101-d8a0-e053-dadaa90a6e4eRitual Antiseptic Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55029-005-01Ritual Antiseptic Hand Sanitizer10 mL in 1 BOTTLELIQUID101
55029-005-02Ritual Antiseptic Hand Sanitizer20 mL in 1 BOTTLELIQUID201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55029-005RITUAL ANTISEPTIC HAND SANITIZER (HAND SANITIZER) LIQUID [SHENZHEN DERUN'EN SCIENCE & TECHNOLOGY DEVELOPMENT CO., LTD]1Legacy NDC, 2 package rows20210124_b97c05dc-9db5-e0c3-e053-2995a90a99e9.zip

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
55029-00555029-005-01, 55029-005-02

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
b97c0445-966b-e750-e053-2995a90a8517b97c05dc-9db5-e0c3-e053-2995a90a99e92021-01-22WarningsExact identifier
spl id: b97c0445-966b-e750-e053-2995a90a8517
spl set id: b97c05dc-9db5-e0c3-e053-2995a90a99e9

Reported adverse events (FAERS/openFDA)#

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