Foaming Alcohol Hand Sanitizer
Alcohol
Betco Corp
Human Otc Drug
NDC 65601-309Foaming Alcohol Hand Sanitizer also known as Alcohol is a human otc drug labeled by 'Betco Corp'. National Drug Code (NDC) number for Foaming Alcohol Hand Sanitizer is 65601-309. This drug is available in dosage form of Aerosol, Foam. The names of the active, medicinal ingredients in Foaming Alcohol Hand Sanitizer drug includes Alcohol - 63 mL/100mL . The currest status of Foaming Alcohol Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 65601-309 |
| 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: | Foaming Alcohol 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: | Alcohol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Betco Corp |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Aerosol, Foam |
| 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 - 63 mL/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: | 08 Jun, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 16 Jan, 2025 |
| 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: | Betco Corp
|
| 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: | 0700427028211
|
| UPC stands for Universal Product Code. |
| 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 |
|---|
| 65601-309-01 | 1 mL in 1 BOTTLE (65601-309-01) | 08 Jun, 2020 | N/A | No |
| 65601-309-02 | 222 mL in 1 BOTTLE (65601-309-02) | 08 Jun, 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 antiseptic
Product Elements:
Foaming alcohol hand sanitizer alcohol .alpha.-tocopherol acetate trolamine glycerin water alcohol alcohol
Indications and Usage:
Directions shake well before using. spray product on hands, enough to cover all surfaces. rub hands together until all surfaces are wet and fully covered. continue rubbing untiil hands feel dry. do not rinse or wipe off sanitizer. supervise children under 6 years of age when using this product to avoid swallowing.
Warnings:
Warnings warnings for external use only do not puncture or incinerate. do not store above 120°f (49°c). when using this product avoid contact with eyes. it splashed in eyes, rinse immediately and thoroughly with water. do not use on chil'dren under 2 months of age. do not use on open wounds. discontinue use if irritation/redness occurs. stop use and ask a physician stop use and ask a physician if irritation occurs for more than 3 days, contact a physician. keep out of reach of children in case of ingestion, get medical help or contact a poison control center immediately.
When Using:
When using this product avoid contact with eyes. it splashed in eyes, rinse immediately and thoroughly with water. do not use on chil'dren under 2 months of age. do not use on open wounds. discontinue use if irritation/redness occurs.
Dosage and Administration:
Dosage & administration spray product on hands, enough to cover all surfaces. rub hands together until all surfaces are wet and fully covered. continue rubbing untiil hands feel dry. do not rinse or wipe off sanitizer.
Stop Use:
Stop use and ask a physician stop use and ask a physician if irritation occurs for more than 3 days, contact a physician.
Package Label Principal Display Panel:
Principal display panel 799e6