Triderma Moisturizing Hand Sanitizer
Alcohol
Genuine Virgin Aloe Corporation
Human Otc Drug
NDC 10738-173Triderma Moisturizing Hand Sanitizer also known as Alcohol is a human otc drug labeled by 'Genuine Virgin Aloe Corporation'. National Drug Code (NDC) number for Triderma Moisturizing Hand Sanitizer is 10738-173. This drug is available in dosage form of Gel. The names of the active, medicinal ingredients in Triderma Moisturizing Hand Sanitizer drug includes Alcohol - .62 mL/mL . The currest status of Triderma Moisturizing Hand Sanitizer drug is Active.
Drug Information:
| Drug NDC: | 10738-173 |
| 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: | Triderma Moisturizing 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: | Genuine Virgin Aloe Corporation |
| 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 - .62 mL/mL
|
| 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 May, 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: | 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, 2024 |
| 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: | Genuine Virgin Aloe Corporation
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 581660
|
| 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. |
| UPC: | 0818926014120
0818926013208
0818926014137
|
| 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 |
|---|
| 10738-173-25 | 65 mL in 1 TUBE (10738-173-25) | 01 May, 2020 | N/A | No |
| 10738-173-45 | 118 mL in 1 TUBE (10738-173-45) | 01 May, 2020 | N/A | No |
| 10738-173-82 | 236 mL in 1 BOTTLE, PUMP (10738-173-82) | 01 May, 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 antimicrobial
Product Elements:
Triderma moisturizing hand sanitizer alcohol aloe vera leaf glycerin isopropyl myristate water .alpha.-tocopherol acetate, dl- alcohol alcohol
Indications and Usage:
Uses âhand sanitizer to help reduce bacteria on the skin that could cause disease. for use when soap and water are not available. recommended for repeated use. ndc 10738-173-82 âhand sanitizer to help reduce bacteria on the skin. for use when soap and water are not available. recommended for repeated use.
Warnings:
Warnings flammable , keep away from fire or flame. for external use only when using this product keep out of eyes, ears and mouth. in case of contact rinse thoroughly with water. avoid contact with broken skin. 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.
When Using:
When using this product keep out of eyes, ears and mouth. in case of contact rinse thoroughly with water. avoid contact with broken skin.
Dosage and Administration:
Directions place enough product in your palm to thoroughly cover your hands. rub hands together until dry. for children under 6, use only under adult supervision. not recommended for infants.
Stop Use:
Stop use and ask a doctor if irritation or rash appears and lasts.
Package Label Principal Display Panel:
Labels 2.2 fl. oz. (65 ml) - ndc 10738-173-25 triderma md® moisturizing hand sanitizer kills 99% of germs* helps reduce bacteria that could cause disease aloe & vitamin e ethyl alcohol antimicrobial experts in skin healing since 1992 *kills 99.9% of most common germs that may cause illness in as little as 15 seconds triderma.com dist. by: genuine virgin aloe corp. corona, ca 92879 ©2020 item 173225 ndc 10738-173-25 4 fl. oz. (118 ml) - ndc 10738-173-45 triderma md® moisturizing hand sanitizer kills 99% of germs* helps reduce bacteria that could cause disease aloe & vitamin e ethyl alcohol antimicrobial experts in skin healing since 1992 *kills 99.9% of most common germs that may cause illness in as little as 15 seconds triderma.com dist. by: genuine virgin aloe corp. corona, ca 92879 ©2020 item 173045 ndc 10738-173-45 8 fl. oz. (236 ml) - ndc 10738-173-82 triderma md® moisturizing hand sanitizer leaves hands feeling soft aloe & vitamin e ethyl alcohol antimicrobial experts in skin healing since 1992 ⢠contains 62% ethyl alcohol ⢠enriched with moisturizing aloe, glycerin & vitamin e ⢠perfect to use when soap & water are not available ⢠dries quickly & leaves hands feeling soft & refreshed triderma.com dist. by: genuine virgin aloe corp. corona, ca 92879 ©2020 item 173082-a ndc 10738-173-82 2.2 fl oz 4 fl oz 8 fl oz
Further Questions:
Questions? 1-800-279-7282 m-f 8am-4pm pst