NDC 21130-145 Signature Care Hand Sanitizer Wipes With Aloe Vera


NDC Product Code 21130-145

NDC CODE: 21130-145

Proprietary Name: Signature Care Hand Sanitizer Wipes 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: 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

  • 21130 - Better Living Brands Llc
    • 21130-145 - Signature Care Hand Sanitizer Wipes With Aloe Vera

NDC 21130-145-02

Package Description: 24 POUCH in 1 PACKAGE > 4.55 g in 1 POUCH (21130-145-01)

NDC Product Information

Signature Care Hand Sanitizer Wipes With Aloe Vera with NDC 21130-145 is a a human over the counter drug product labeled by Better Living Brands Llc. The generic name of Signature Care Hand Sanitizer Wipes With Aloe Vera is alcohol. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Better Living Brands Llc

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.

Signature Care Hand Sanitizer Wipes 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 70 g/100g

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.

  • WATER (UNII: 059QF0KO0R)

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: Better Living Brands Llc
Labeler Code: 21130
FDA Application Number: part333E 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: 04-14-2021 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.

Signature Care Hand Sanitizer Wipes With Aloe Vera Product Label Images

Signature Care Hand Sanitizer Wipes 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% v/v




  • For hand washing to decrease bacteria on the skin.Recommended for repeaed use.Dries in seconds.


  • For external use onlyFlammable.Keep away from fire and flame.When using this productAvoid contact with eyes. In case of contact with eyes, fllush thoroughly with water.Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a physician.Other InformationLot No. and Expiration date can be found on packet.

Keep Out Of Reach Of Children.

  • Unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.


  • Tear open packet.Open and unfold wipe.Thoroughly wipe hands, fingers and wrists. Be sure to use the entire wipe.For dirty hads, use first wipe to clean hands, then discard wipe; sanitize with second wipe.Discard after single use.

Inactive Ingredients

Water, Glycerin, Aloe Barbadensis Leaf Extract

* Please review the disclaimer below.