Yenaya Secret Gung Cleanser
Cocamidopropyl Betaine, Lactic Acid
Ifackorea Co., Ltd
Human Otc Drug
NDC 81873-202Yenaya Secret Gung Cleanser also known as Cocamidopropyl Betaine, Lactic Acid is a human otc drug labeled by 'Ifackorea Co., Ltd'. National Drug Code (NDC) number for Yenaya Secret Gung Cleanser is 81873-202. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Yenaya Secret Gung Cleanser drug includes Cocamidopropyl Betaine - 8 mg/100mL Lactic Acid, Unspecified Form - 1 mg/100mL . The currest status of Yenaya Secret Gung Cleanser drug is Active.
Drug Information:
| Drug NDC: | 81873-202 |
| 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: | Yenaya Secret Gung Cleanser |
| 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: | Cocamidopropyl Betaine, Lactic Acid |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Ifackorea Co., Ltd |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Gel |
| 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: | COCAMIDOPROPYL BETAINE - 8 mg/100mL
LACTIC ACID, UNSPECIFIED FORM - 1 mg/100mL
|
| 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: | UNAPPROVED DRUG OTHER |
| 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: | 06 May, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 May, 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. |
| 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: | IFACKOREA 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. |
| NUI: | N0000175833
|
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). |
| UNII: | 5OCF3O11KX
33X04XA5AT
|
| 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. |
| Pharmacologic Class MOA: | Acidifying Activity [MoA]
|
| Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`. |
| Pharmacologic Class: | Acidifying Activity [MoA]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 81873-202-01 | 100 mL in 1 BOTTLE, PUMP (81873-202-01) | 06 May, 2021 | 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 surfactant anti-bacterial
Product Elements:
Yenaya secret gung cleanser cocamidopropyl betaine, lactic acid scutellaria baicalensis root 4-(p-hydroxyphenyl)-2-butanone artemisia princeps leaf salix alba bark oregano purslane edetate disodium anhydrous .beta.-citronellol, (r)- benzyl salicylate eugenol phenylethyl alcohol linalool, (+/-)- chinese cinnamon phenylisohexanol triethanolamine cocoyl glutaminate geraniol chamaecyparis obtusa leaf allantoin water disodium laureth sulfosuccinate .alpha.-hexylcinnamaldehyde corchorus olitorius leaf ethylhexylglycerin cocamidopropyl betaine cocamidopropyl betaine glycerin pistacia lentiscus resin oil ethylene glycol monobenzyl ether lactic acid, unspecified form lactic acid, unspecified form menthol, unspecified form
Indications and Usage:
Directions pour into hand and apply. rinse thoroughly with warm water.
Warnings:
Warnings for external use only
When Using:
When using this product avoid contact with eyes, in case of contact, rinse eyes thoroughly with water.
Dosage and Administration:
Uses essentials for femaleâs hygiene and more. gentle cleanses and freshens. removes odor causing bacteria. work smoothly to keep femaleâs sensitive area slightly acidic condition. frequent use does not affect sensitive skin at all.
Stop Use:
Stop use and ask doctor if irritation or persistent itching.
Package Label Principal Display Panel:
Package label 81873-201-01