DR.URBAN V ZERO HAND CLEANER- hypochlorous acid spray

Dr.URBAN V Zero Hand Cleaner by

Drug Labeling and Warnings

Dr.URBAN V Zero Hand Cleaner by is a Otc medication manufactured, distributed, or labeled by Lizcos Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients: Hypochlorous Acid 99.0%

INACTIVE INGREDIENT

Inactive ingredients:

Centella Asiatica Extract, Saururus Chinensis Extract, Glycerin, PEG-60 Hydrogenated Castor Oil, Fragrance

PURPOSE

Purpose: disinfectant

WARNINGS

Warnings:

For external use only. Flammable. Keep away from heat or flame
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Do not use
in children less than 2 months of age
on open skin wounds
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Uses:

Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

Directions:

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.URBAN V ZERO HAND CLEANER 
hypochlorous acid spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76895-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Hypochlorous Acid (UNII: 712K4CDC10) (Hypochlorous Acid - UNII:712K4CDC10)	Hypochlorous Acid	495 g  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
Glycerin (UNII: PDC6A3C0OX)
PEG-60 Hydrogenated Castor Oil (UNII: 02NG325BQG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76895-020-01	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2020

Labeler - Lizcos Co.,Ltd. (694708474)

Registrant - Lizcos Co.,Ltd. (694708474)

Establishment
Name	Address	ID/FEI	Business Operations
Lizcos Co.,Ltd.		694708474	manufacture(76895-020)