Forticept Antimicrobial Hydrogel Wound Dressing
Benzethonium Chloride, Thymol
Lidan, Inc
Human Otc Drug
NDC 72127-0901Forticept Antimicrobial Hydrogel Wound Dressing also known as Benzethonium Chloride, Thymol is a human otc drug labeled by 'Lidan, Inc'. National Drug Code (NDC) number for Forticept Antimicrobial Hydrogel Wound Dressing is 72127-0901. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Forticept Antimicrobial Hydrogel Wound Dressing drug includes Benzethonium Chloride - 1 g/1000g Thymol - 1 g/1000g . The currest status of Forticept Antimicrobial Hydrogel Wound Dressing drug is Active.
Drug Information:
| Drug NDC: | 72127-0901 |
| 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: | Forticept Antimicrobial Hydrogel Wound Dressing |
| 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: | Benzethonium Chloride, Thymol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Lidan, Inc |
| 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: | BENZETHONIUM CHLORIDE - 1 g/1000g
THYMOL - 1 g/1000g
|
| 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 NOT 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: | 20 Feb, 2022 |
| 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: | part333A |
| 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: | Lidan, Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 2044644
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | PH41D05744
3J50XA376E
|
| 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 |
|---|
| 72127-0901-1 | 85 g in 1 TUBE (72127-0901-1) | 20 Feb, 2022 | 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:
Uses helps protect skin and supports healing of minor cuts, scrapes, burns and wounds, including pressure sores, diabetic ulcers, cracked skin and lips. topical antiseptic to help decrease the risk of skin infections.
Product Elements:
Forticept antimicrobial hydrogel wound dressing benzethonium chloride, thymol benzethonium chloride benzethonium thymol thymol sodium acrylate/sodium acryloyldimethyltaurate copolymer (4000000 mw) allantoin .alpha.-tocopherol acetate, dl- cetostearyl alcohol dexpanthenol glycerin hydrolysed bovine collagen (enzymatic; 2000-5000 mw) isohexadecane lanolin mineral oil petrolatum polihexanide polysorbate 80 shea butter steareth-2 steareth-21 water
Indications and Usage:
Do not use on children under 2 years of age unless directed by a doctor. when using this product avoid contact with eyes.
Warnings:
Warnings for external use only.
Dosage and Administration:
Directions: adults and children 2 years of age and older: clean affected area from dirt and debris, let it dry. apply a thin layer of forticept antimicrobial gel and cover affected area with a clean bandage if needed. repeat this procedure 1-3 times daily or as needed until condition improves. children under 2 years of age: please, consult a doctor
Stop Use:
Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.
Package Label Principal Display Panel:
85g tube 85g tube