Aloesafe Antiseptic Hand Sanitizer
Ethyl Alcohol
Medical Chemical Corporation
Human Otc Drug
NDC 12745-180Aloesafe Antiseptic Hand Sanitizer also known as Ethyl Alcohol is a human otc drug labeled by 'Medical Chemical Corporation'. National Drug Code (NDC) number for Aloesafe Antiseptic Hand Sanitizer is 12745-180. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Aloesafe Antiseptic Hand Sanitizer drug includes Alcohol - 60 g/100mL . The currest status of Aloesafe Antiseptic Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 12745-180 |
| 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: | Aloesafe Antiseptic Hand Sanitizer |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Aloesafe |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | Antiseptic Hand Sanitizer |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| 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: | Ethyl Alcohol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Medical Chemical Corporation |
| 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: | ALCOHOL - 60 g/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: | 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 Jul, 2010 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 23 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: | part333E |
| 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: | Medical Chemical Corporation
|
| 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: | 3K9958V90M
|
| 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 |
|---|
| 12745-180-01 | 60 mL in 1 BOTTLE, PLASTIC (12745-180-01) | 14 Oct, 2019 | N/A | No |
| 12745-180-02 | 120 mL in 1 BOTTLE, PLASTIC (12745-180-02) | 01 Jul, 2010 | N/A | No |
| 12745-180-03 | 480 mL in 1 BOTTLE, PLASTIC (12745-180-03) | 01 Jul, 2010 | 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:
Indications for use indications for use: aloesafe is intended to be used as a waterless hand sanitizer to reduce microorganisms that can cause disease. recommended fo repeated use.
Product Elements:
Aloesafe antiseptic hand sanitizer ethyl alcohol polyacrylic acid (450000 mw) aloe vera leaf lavender oil alpha-tocopherol acetate water alcohol alcohol diisopropylamine
Indications and Usage:
Indications for use indications for use: aloesafe is intended to be used as a waterless hand sanitizer to reduce microorganisms that can cause disease. recommended fo repeated use.
Warnings:
Warnings warnings: flammable, keep away from fire or flames. for external use on hands only. avoid contact with face, eyes and broken skin. if this occurs, flush thoroughly with water. discontinue use if irritation or redness develops. keep out of reach of children. in case of ingestion contact poison control center immediately.
Warnings and Cautions:
Warnings warnings: flammable, keep away from fire or flames. for external use on hands only. avoid contact with face, eyes and broken skin. if this occurs, flush thoroughly with water. discontinue use if irritation or redness develops. keep out of reach of children. in case of ingestion contact poison control center immediately.
Dosage and Administration:
Directions directions: wet hands thoroughly with aloesafe and rub briskly until dry without wiping.
Package Label Principal Display Panel:
Aloesafe label aloesafe label