Purupuru Hand Sanitizer
Alcohol
Jyoungcosmetic Inc.
Human Otc Drug
NDC 79547-201Purupuru Hand Sanitizer also known as Alcohol is a human otc drug labeled by 'Jyoungcosmetic Inc.'. National Drug Code (NDC) number for Purupuru Hand Sanitizer is 79547-201. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Purupuru Hand Sanitizer drug includes Alcohol - 71.25 mL/100mL . The currest status of Purupuru Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 79547-201 |
| 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: | Purupuru 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: | Jyoungcosmetic 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 - 71.25 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: | 10 Jul, 2020 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 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: | Jyoungcosmetic 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: | 8809747050000
8809747050468
8809747050475
|
| 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 |
|---|
| 79547-201-01 | 500 mL in 1 BOTTLE, PUMP (79547-201-01) | 10 Jul, 2020 | N/A | No |
| 79547-201-02 | 30 mL in 1 BOTTLE (79547-201-02) | 10 Jul, 2020 | N/A | No |
| 79547-201-03 | 50 mL in 1 BOTTLE (79547-201-03) | 10 Jul, 2020 | N/A | No |
| 79547-201-04 | 100 mL in 1 BOTTLE (79547-201-04) | 10 Jul, 2020 | N/A | No |
| 79547-201-05 | 250 mL in 1 BOTTLE (79547-201-05) | 10 Jul, 2020 | N/A | No |
| 79547-201-06 | 300 mL in 1 BOTTLE (79547-201-06) | 10 Jul, 2020 | N/A | No |
| 79547-201-07 | 500 mL in 1 BOTTLE, PUMP (79547-201-07) | 10 Jul, 2020 | N/A | No |
| 79547-201-08 | 50 mL in 1 BOTTLE (79547-201-08) | 10 Jul, 2020 | N/A | No |
| 79547-201-09 | 100 mL in 1 BOTTLE (79547-201-09) | 10 Jul, 2020 | N/A | No |
| 79547-201-10 | 60 mL in 1 BOTTLE (79547-201-10) | 10 Jul, 2020 | N/A | No |
| 79547-201-11 | 1000 mL in 1 BOTTLE, PUMP (79547-201-11) | 10 Jul, 2020 | N/A | No |
| 79547-201-12 | 5000 mL in 1 BOTTLE, PLASTIC (79547-201-12) | 10 Jul, 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:
Purupuru hand sanitizer alcohol trolamine hyaluronate sodium centella asiatica butylene glycol carbomer interpolymer type a (55000 cps) 1,2-hexanediol carbomer homopolymer, unspecified type alcohol alcohol water green tea leaf aloe vera leaf
Indications and Usage:
Directions place enough product on hands to cover all surfaces. rub hands together until dry. supervise children under 6 years of age when using this product to avoid swallowing.
Warnings:
Warnings for external use only, flammable, keep away from heat or flame.
Do Not Use:
Warnings for external use only, flammable, keep away from heat or flame.
When Using:
When using this product keep out of eyes, ears, and mouth. in case of contact with eyes, rinse eyes thoroughly with water.
Dosage and Administration:
Uses hand sanitizer to help reduce bacteria that potentially can cause disease. for use when soap and water are not available.
Package Label Principal Display Panel:
Package label 500ml ndc: 79547-201-01 label 30ml ndc: 79547-201-02 label 50ml ndc: 79547-201-03 label 100ml ndc: 79547-201-04 label 250ml ndc: 79547-201-05 label 300ml ndc: 79547-201-06 label 500ml ndc: 79547-201-07 label 50ml ndc: 79547-201-08 label 100ml ndc: 79547-201-09 label 60ml ndc: 79547-201-10 label 79547-201-11 79547-201-12