NDC 74741-0023 Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera

Ethyl Alcohol

NDC Product Code 74741-0023

NDC CODE: 74741-0023

Proprietary Name: Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Ethyl Alcohol What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 74741 - Mprbrain Co.ltd
    • 74741-0023 - Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera

NDC 74741-0023-1

Package Description: 20 CLOTH in 1 PACKET

NDC Product Information

Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera with NDC 74741-0023 is a a human over the counter drug product labeled by Mprbrain Co.ltd. The generic name of Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera is ethyl alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Mprbrain Co.ltd

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 3.325 g/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)
  • HYALURONIC ACID (UNII: S270N0TRQY)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Mprbrain Co.ltd
Labeler Code: 74741
FDA Application Number: part333A What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 03-25-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera Product Label Images

Dr. Yerma Sanitizer Wipes Cool Scented With Aloe Vera Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Ethyl alcohol 70 %

Purpose

Antiseptic

Other Information

Do not store above 86 °Fmay discolor some fabricsharmful to wood finishes and plastics

Inactive Ingredients

Aqua, Glycerin, Hyaluronic Acid, Aloe Barbadensis Leaf Extract, Fragrance

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

When Using This Product

Keep out of eyes. In case of contact with eyes, flush thoroughly with water.avoid contact with broken skin.do not inhale or ingest.

Directions

Use towelette to thoroughly wipe hands or surfacesfor children under 6, use only under adult supervisionnot recommended for infants

Warnings

For external use only: handsFlammable, keep away from fire or flame.

Stop Use And Ask A Doctor If

Irritation or redness developsconditions persists for more than 72 hours

* Please review the disclaimer below.