NDC 71939-004 Zudaifu Antibacterial Cream

Zudaifu Antibacterial Cream

NDC Product Code 71939-004

NDC CODE: 71939-004

Proprietary Name: Zudaifu Antibacterial Cream 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: Zudaifu Antibacterial Cream 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

  • 71939 - Taizhou Youpeng Import And Export Trading Co.,ltd.

NDC 71939-004-01

Package Description: 15 g in 1 PACKAGE, COMBINATION

NDC Product Information

Zudaifu Antibacterial Cream with NDC 71939-004 is a a human over the counter drug product labeled by Taizhou Youpeng Import And Export Trading Co.,ltd.. The generic name of Zudaifu Antibacterial Cream is zudaifu antibacterial cream. The product's dosage form is salve and is administered via topical form.

Labeler Name: Taizhou Youpeng Import And Export Trading Co.,ltd.

Dosage Form: Salve - A thick ointment or cerate (a fat or wax based preparation with a consistency between an ointment and a plaster).

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.

Zudaifu Antibacterial Cream 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.

  • SOPHORA FLAVESCENS ROOT 75 mg/15g
  • CNIDIUM MONNIERI FRUIT 30 mg/15g
  • STEMONA SESSILIFOLIA ROOT 30 mg/15g
  • CHLORHEXIDINE ACETATE 37.5 mg/15g

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.

  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y)
  • MENTHONE, (+/-)- (UNII: 9NH5J4V8FN)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • 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.
  • 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: Taizhou Youpeng Import And Export Trading Co.,ltd.
Labeler Code: 71939
Marketing Category: UNAPPROVED DRUG OTHER - 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: 07-15-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Zudaifu Antibacterial Cream Product Label Images

Zudaifu Antibacterial Cream 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

Dosage & Administration

Keep it sealed in a cool and dry place

Inactive Ingredient

KOCHIAEFRUCTUS,Stearic Acid,Petrolatum, Purified Water.Menthone

Indications & Usage

Apply the product to skin discomfort area.

Otc - Active Ingredient

Chlorhexldine AcetateSOPHORAEFLAVESGEMTIS RADIXCNIDII FRUCTUSSTEMONAE RADI

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Otc - Purpose

Disinfection

Sterilization

No Rinseing

Warnings

1.Forbidden for people who are aleric to the product and any of its ingredients.

2.if the product character changes, don't use it.

3.Please place the product in the place where children can not reach.

4.Don't use this product on injured skin, mucous membrane,wounds.

5.This product is not a substitute for medicine.

* Please review the disclaimer below.