HEALTHA CLEAN- calcium undecylenate liquid
Ventex Co., Ltd

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredients

Calcium undecylenate

Purpose

Antimicrobial

Inactive Ingredients

water, malic acid,Glycine

Directions

it is a violation of Federal law to use this product in a manner inconsistent with its labeling.

hold container 6"-8" from surface and spray until thoroughly wet then allow to air dry.

Do not use

in children less than 2 months of age.

on open skin wounds

when using

our disinfectant can be used to eliminate germs- on commonly touched hard & soft surfaces and also deodorizes places in which it is present by degrading harmful gases in the air.

Stop use and ask a doctor

in case of eye contact, immediately flush eyes with water. if swallowed, contact physician.

warnings

do not place in direct sunlight or where there may be serve temperature changes.

keep out of rech of children

use

heltha clean disintectant spray kills of the viruses and bacteria your family comes in contact with every day.

Other information

This can be carried in a pocket or bag for easy and multiple uses on fabric and products which need to be disinfected.

Package Label

100g 500g

HEALTHA CLEAN
calcium undecylenate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75377-301
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM UNDECYLENATE (UNII: 77YW1RTU8V) (CALCIUM UNDECYLENATE - UNII:77YW1RTU8V)	CALCIUM UNDECYLENATE	1 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
ZINC OXIDE (UNII: SOI2LOH54Z)	0.8 g in 100 g
GLYCINE (UNII: TE7660XO1C)	0.2 g in 100 g
MALIC ACID (UNII: 817L1N4CKP)	0.2 g in 100 g
WATER (UNII: 059QF0KO0R)	97.8 g in 100 g

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:75377-301-01	500 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020
2	NDC:75377-301-02	100 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/24/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333C	04/24/2020

Labeler - Ventex Co., Ltd (688813182)

Registrant - Ventex Co., Ltd (688813182)

Name	Address	ID/FEI	Business Operations
Establishment
Ventex Co., Ltd		688813182	manufacture(75377-301)

Revised: 12/2022

Document Id: efebb4d7-8ae9-9564-e053-2a95a90a3a7b

Set id: a33db6d2-8587-196b-e053-2a95a90ad7ec

Version: 5

Effective Time: 20221215

Ventex Co., Ltd