Puroma Hand Sanitizer Fragrance Free

Alcohol


Zenith Micro Control
Human Otc Drug
NDC 80948-010
Puroma Hand Sanitizer Fragrance Free also known as Alcohol is a human otc drug labeled by 'Zenith Micro Control'. National Drug Code (NDC) number for Puroma Hand Sanitizer Fragrance Free is 80948-010. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Puroma Hand Sanitizer Fragrance Free drug includes Alcohol - 75 mL/100mL . The currest status of Puroma Hand Sanitizer Fragrance Free drug is Active.

Drug Information:

Drug NDC: 80948-010
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: Puroma Hand Sanitizer Fragrance Free
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: Zenith Micro Control
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 - 75 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: 12 Mar, 2021
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 07 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:ZENITH MICRO CONTROL
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 NDCDescriptionMarketing Start DateMarketing End DateSample Available
80948-010-332 PACKAGE in 1 PACKAGE (80948-010-33) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-344 PACKAGE in 1 PACKAGE (80948-010-34) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-356 PACKAGE in 1 PACKAGE (80948-010-35) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-368 PACKAGE in 1 PACKAGE (80948-010-36) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-3712 PACKAGE in 1 PACKAGE (80948-010-37) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-3824 PACKAGE in 1 PACKAGE (80948-010-38) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-3948 PACKAGE in 1 PACKAGE (80948-010-39) / 350 mL in 1 PACKAGE12 Mar, 2021N/ANo
80948-010-402 BOTTLE in 1 PACKAGE (80948-010-40) / 500 mL in 1 BOTTLE12 Mar, 2021N/ANo
80948-010-414 BOTTLE in 1 PACKAGE (80948-010-41) / 500 mL in 1 BOTTLE12 Mar, 2021N/ANo
80948-010-426 BOTTLE in 1 PACKAGE (80948-010-42) / 500 mL in 1 BOTTLE12 Mar, 2021N/ANo
80948-010-435000 mL in 1 CAN (80948-010-43)12 Mar, 2021N/ANo
80948-010-4450000 mL in 1 CAN (80948-010-44)12 Mar, 2021N/ANo
80948-010-45200000 mL in 1 DRUM (80948-010-45)12 Mar, 2021N/ANo
80948-010-466 BOTTLE in 1 PACKAGE (80948-010-46) / 30 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-478 BOTTLE in 1 PACKAGE (80948-010-47) / 30 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-4812 BOTTLE in 1 PACKAGE (80948-010-48) / 30 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-4924 BOTTLE in 1 PACKAGE (80948-010-49) / 30 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-5048 BOTTLE in 1 PACKAGE (80948-010-50) / 30 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-516 BOTTLE in 1 PACKAGE (80948-010-51) / 50 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-528 BOTTLE in 1 PACKAGE (80948-010-52) / 50 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-5312 BOTTLE in 1 PACKAGE (80948-010-53) / 50 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-5424 BOTTLE in 1 PACKAGE (80948-010-54) / 50 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-5548 BOTTLE in 1 PACKAGE (80948-010-55) / 50 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-566 BOTTLE in 1 PACKAGE (80948-010-56) / 60 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-578 BOTTLE in 1 PACKAGE (80948-010-57) / 60 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-5812 BOTTLE in 1 PACKAGE (80948-010-58) / 60 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-5924 BOTTLE in 1 PACKAGE (80948-010-59) / 60 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-6048 BOTTLE in 1 PACKAGE (80948-010-60) / 60 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-616 BOTTLE in 1 PACKAGE (80948-010-61) / 100 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-628 BOTTLE in 1 PACKAGE (80948-010-62) / 100 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-6312 BOTTLE in 1 PACKAGE (80948-010-63) / 100 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-6424 BOTTLE in 1 PACKAGE (80948-010-64) / 100 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-6548 BOTTLE in 1 PACKAGE (80948-010-65) / 100 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-664 BOTTLE in 1 PACKAGE (80948-010-66) / 200 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-676 BOTTLE in 1 PACKAGE (80948-010-67) / 200 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-688 BOTTLE in 1 PACKAGE (80948-010-68) / 200 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-6912 BOTTLE in 1 PACKAGE (80948-010-69) / 200 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-7024 BOTTLE in 1 PACKAGE (80948-010-70) / 200 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-7148 BOTTLE in 1 PACKAGE (80948-010-71) / 200 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-724 BOTTLE in 1 PACKAGE (80948-010-72) / 250 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-736 BOTTLE in 1 PACKAGE (80948-010-73) / 250 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-748 BOTTLE in 1 PACKAGE (80948-010-74) / 250 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-7512 BOTTLE in 1 PACKAGE (80948-010-75) / 250 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-7624 BOTTLE in 1 PACKAGE (80948-010-76) / 250 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-7748 BOTTLE in 1 PACKAGE (80948-010-77) / 250 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-782 BOTTLE in 1 PACKAGE (80948-010-78) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-794 BOTTLE in 1 PACKAGE (80948-010-79) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-806 BOTTLE in 1 PACKAGE (80948-010-80) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-818 BOTTLE in 1 PACKAGE (80948-010-81) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-8212 BOTTLE in 1 PACKAGE (80948-010-82) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-8324 BOTTLE in 1 PACKAGE (80948-010-83) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-8448 BOTTLE in 1 PACKAGE (80948-010-84) / 350 mL in 1 BOTTLE19 Oct, 2021N/ANo
80948-010-8550 mL in 1 BOTTLE (80948-010-85)19 Oct, 2021N/ANo
80948-010-86200 mL in 1 BOTTLE (80948-010-86)19 Oct, 2021N/ANo
80948-010-87100 mL in 1 BOTTLE (80948-010-87)19 Oct, 2021N/ANo
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 antimicrobial.

Product Elements:

Puroma hand sanitizer fragrance free alcohol water isopropyl alcohol glycerin isopropyl myristate alpha-tocopherol acetate caprylyl glycol aloe vera leaf propylene glycol coco-caprylate glyceryl oleate peg-7 glyceryl cocoate alcohol alcohol

Indications and Usage:

Uses hand sanitizer to help reduce bacteria on skin that potentially can cause disease. for use when soap and water are not available.

Warnings:

Warnings • flammable. keep away from fire or flame. • when using this product do not use in or near the eyes. in case of contact, rinse eyes thoroughly with water. • stop use and ask a doctor if irritation or rash appears and lasts.

Dosage and Administration:

Directions spray enough product on hands to cover all surfaces. rub hands together briskly until dry. children under 6 years of age should be supervised when using puroma hand sanitizer

Package Label Principal Display Panel:

Product label image description


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.