Healtha Clean
Calcium Undecylenate
Ventex Co., Ltd
Human Otc Drug
NDC 75377-301Healtha Clean also known as Calcium Undecylenate is a human otc drug labeled by 'Ventex Co., Ltd'. National Drug Code (NDC) number for Healtha Clean is 75377-301. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Healtha Clean drug includes Calcium Undecylenate - 1 g/100g . The currest status of Healtha Clean drug is Active.
Drug Information:
| Drug NDC: | 75377-301 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Healtha Clean |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Calcium Undecylenate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Ventex Co., Ltd |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | CALCIUM UNDECYLENATE - 1 g/100g
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 24 Apr, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 19 Jun, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part333C |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | Ventex Co., Ltd
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 77YW1RTU8V
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 75377-301-01 | 500 g in 1 BOTTLE, SPRAY (75377-301-01) | 24 Apr, 2020 | N/A | No |
| 75377-301-02 | 100 g in 1 BOTTLE, SPRAY (75377-301-02) | 24 Apr, 2020 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose antimicrobial
Product Elements:
Healtha clean calcium undecylenate zinc oxide glycine malic acid calcium undecylenate calcium undecylenate water
Indications and Usage:
Use heltha clean disintectant spray kills of the viruses and bacteria your family comes in contact with every day.
Warnings:
Warnings do not place in direct sunlight or where there may be serve temperature changes.
Do Not Use:
Warnings do not place in direct sunlight or where there may be serve temperature changes.
When Using:
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.
Dosage and Administration:
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.
Package Label Principal Display Panel:
Package label 100g 500g