Active Ingredient(S)
Benzalkonium Chloride 0.13%
Ritual Antiseptic Hand Sanitizer
FDA Label NDC 55029-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Derun'en Science & Technology Development Co., Ltd for the product Ritual Antiseptic Hand Sanitizer (NDC 55029-005). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use, warnings, keep out of reach of childen, directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For hand washing to decrease bacteria on the skin
Warnings
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
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping
Inactive Ingredients
Deionized water
Other Information
Importer info:
Essence 360
5778 Boulevard Thimens, Saint-Laurent, QC, H4R 2K9, Canada
Package Label - Principal Display Panel
10ML IN 1 BOTTLE NDC:55029-005-01
Label-10ml (Label 10ml)
20ML IN 1 BOTTLE NDC:55029-005-02
Label-20ml (Label 20ml)
* Please review the disclaimer below.
