Dermaphex Hand Sanitizer
Aphex Biocleanse Systems, Inc
Human Otc Drug
NDC 78003-120Dermaphex Hand Sanitizer is a human otc drug labeled by 'Aphex Biocleanse Systems, Inc'. National Drug Code (NDC) number for Dermaphex Hand Sanitizer is 78003-120. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Dermaphex Hand Sanitizer drug includes Benzalkonium Chloride - .0013 g/mL . The currest status of Dermaphex Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 78003-120 |
| 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: | Dermaphex Hand Sanitizer |
| 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: | Dermaphex Hand Sanitizer |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Aphex Biocleanse Systems, Inc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Solution |
| 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: | BENZALKONIUM CHLORIDE - .0013 g/mL
|
| 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: | 01 Jun, 2012 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 04 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. |
| 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: | Aphex Biocleanse Systems, Inc
|
| 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. |
| UPC: | 0850608003329
|
| UPC stands for Universal Product Code. |
| UNII: | F5UM2KM3W7
|
| 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 |
|---|
| 78003-120-70 | 208000 mL in 1 DRUM (78003-120-70) | 01 Jun, 2012 | N/A | No |
| 78003-120-80 | 1054000 mL in 1 CONTAINER (78003-120-80) | 01 Jun, 2012 | 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 active ingredients: benzalkonium chloride 0.11% - 0 .13% (as sanitizing agent)
Product Elements:
Dermaphex hand sanitizer dermaphex hand sanitizer urea water benzalkonium chloride benzalkonium
Indications and Usage:
Indications and usage uses: for hand sanitizing. helps prevent the risk and spread of infection as well as communicable diseases by killing germs that reside on the surface of the skin.
Warnings:
Warnings warnings: for external use only do not use in eyes. in case of eye contact, immediately flush with water and seek medical advice. discontinue use if skin irritation or redness develops. not for use on sensitive areas of the body or burns. if swallowed, get medical help or contact a poison control center right away. keep out of reach of children
Dosage and Administration:
Dosage and administration directions: refill your container. 1 - 4 pumps into your palm. rub foam until spread evenly over the entire surface of your hands. continue rubbing until dry. use frequently to avoid spreading germs.
Package Label Principal Display Panel:
Dermaphex 275 gallon container dermaphex275gal
Dermaphex 55 gallon dermaphex55gal