Green Key
Hand Sanitizer
Diamond Chemical Co Inc
Human Otc Drug
NDC 72177-187Green Key also known as Hand Sanitizer is a human otc drug labeled by 'Diamond Chemical Co Inc'. National Drug Code (NDC) number for Green Key is 72177-187. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Green Key drug includes Alcohol - 70 mL/100mL . The currest status of Green Key drug is Active.
Drug Information:
| Drug NDC: | 72177-187 |
| 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: | Green Key |
| 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: | Hand Sanitizer |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Diamond Chemical Co 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: | ALCOHOL - 70 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: | 25 Mar, 2021 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 25 Dec, 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: | 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: | Diamond Chemical Co Inc
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 581662
|
| 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: | 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 |
|---|
| 72177-187-31 | 3785 mL in 1 CONTAINER (72177-187-31) | 25 Mar, 2021 | 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 antimicrobial
Product Elements:
Green key hand sanitizer alcohol alcohol acrylates/vinyl isodecanoate crosspolymer (10000 mpa.s neutralized at 0.5%) water
Indications and Usage:
Use hand sanitizer to help decrease bacteria on the skin
Warnings:
Warnings flammable. keep away from fire or flame. for external use only.
Do Not Use:
Warnings flammable. keep away from fire or flame. for external use only.
When Using:
Usage when using this product do not use in or near the eyes, in case of contact rinse eye thoroughly with water. stop use and ask a doctor if irritation or rash appears and lasts. keep out of reach of children if swallowed, get medical help or contact a poison control center right away.
Dosage and Administration:
Directions if hands are visibly soiled, wash with soap and water then dry hands. wet hands thoroughly with product, especially under the fingernails and allow to dry without rinsing. children under 6 years of age should be supervised when using this product.
Stop Use:
Stop use stop use and ask a doctor if irritation or rash appears and lasts.
Package Label Principal Display Panel:
Green key label description kills germs fast leaves hands smooth & refreshed this one step sanitizer kills most disease-causing germs within seconds. use as frequently as wanted and between normal hand washing. green key hand sanitizer contains skin conditioners which leaves hands refreshed and sanitized. green key hand sanitizer reduces the risk of cross infection without having to use soap and water. directions if hands are visibly soiled, wash with soap and water then dry hands. wet hands thoroughly with product, especially under the fingernails and allow to dry without rinsing. children under 6 years of age should be supervised when using this product. green key ® gel instant hand sanitizer use without water new & improved keep out of reach of children mant Ãngase alejado del alcance de los ni Ãos net contents: 1 gallon drug facts active ingredientâ¦â¦â¦.⦠ethyl alcohol 70% v/v purposeâ¦â¦â¦â¦â¦â¦â¦â¦.. â¦antimicrobial use hand sanitizer to help decrease bacteria on the skin warnings flammable. keep away from fire or flame. for external use only. when using this product do not use in or near the eyes, in case of contact rinse eye thoroughly with water. stop use and ask a doctor if irritation or rash appears and lasts. keep out of reach of children if swallowed, get medical help or contact a poison control center right away. other information store below 110°f (43°c) may discolor certain fabrics or surfaces inactive ingredients water (aqua), peg-6, amp-acrylates / vinyl isodecanoate crosspolymer, aloe barbadensis leaf juice, fragrance (parfum). manufactured by: diamond ® chemical company inc. union ave & dubois street east rutherford, nj 07073 (201) 935-4300 tsr:18621 7 65574 18631 3 for chemical & medical emergencies call: 1-800-535-5053 made in the usa green key label