NDC 77435-101 Handy Antibac Antiseptic Hand Sanitizing Wipes

Alcohol

NDC Product Code 77435-101

NDC CODE: 77435-101

Proprietary Name: Handy Antibac Antiseptic Hand Sanitizing Wipes 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

  • 77435 - Haining Lily Cleaning Products Co., Ltd
    • 77435-101 - Handy Antibac Antiseptic Hand Sanitizing Wipes

NDC 77435-101-03

Package Description: 150 PACKAGE in 1 CANISTER > 9.12 g in 1 PACKAGE

NDC Product Information

Handy Antibac Antiseptic Hand Sanitizing Wipes with NDC 77435-101 is a a human over the counter drug product labeled by Haining Lily Cleaning Products Co., Ltd. The generic name of Handy Antibac Antiseptic Hand Sanitizing Wipes is alcohol. The product's dosage form is cloth and is administered via topical form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1307051.

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.

Handy Antibac Antiseptic Hand Sanitizing Wipes 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.


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: Haining Lily Cleaning Products Co., Ltd
Labeler Code: 77435
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: 06-28-2020 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: 12-31-2021 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.

Handy Antibac Antiseptic Hand Sanitizing Wipes Product Label Images

Handy Antibac Antiseptic Hand Sanitizing Wipes 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 75%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin.

Warning

  • 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 eyes thoroughly with water.Stop use and ask a doctor, if irritaion and redness develop; condition persists for ore than 72 hoursOther Information:Do not store above 100℉ (38 ℃)May discolor some fabrics or surface

Otc - Keep Out Of Reach Of Children

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

Directions

  • Wet hands thoroughluy with produt and allow to dry without wiping

Inactive Ingredients

Water, aloe vera

* Please review the disclaimer below.