NDC 73076-133 Wound Care

Wound Care Ointment

NDC Product Code 73076-133

NDC Code: 73076-133

Proprietary Name: Wound Care 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: Wound Care Ointment 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

  • 73076 - Shenzhen Ishan Technology Co.,ltd
    • 73076-133 - Wound Care

NDC 73076-133-01

Package Description: 25 g in 1 BOTTLE

NDC 73076-133-02

Package Description: 50 g in 1 BOTTLE

NDC 73076-133-03

Package Description: 100 g in 1 BOTTLE

NDC 73076-133-04

Package Description: 15 g in 1 BOTTLE

NDC Product Information

Wound Care with NDC 73076-133 is a a human over the counter drug product labeled by Shenzhen Ishan Technology Co.,ltd. The generic name of Wound Care is wound care ointment. The product's dosage form is ointment and is administered via topical form.

Labeler Name: Shenzhen Ishan Technology Co.,ltd

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Wound Care 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.

  • ZINC OXIDE .5 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.

  • PROPOLIS WAX (UNII: 6Y8XYV2NOF)
  • SESAME OIL (UNII: QX10HYY4QV)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • LINOLEIC ACID (UNII: 9KJL21T0QJ)

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: Shenzhen Ishan Technology Co.,ltd
Labeler Code: 73076
FDA Application Number: part347 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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 05-07-2019 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: 12-31-2020 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.

Wound Care 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 Ingredients

Zinc Oxide--0.5%

Inactive Ingredients

Bees Wax, Linoleic Acid, Propolis, Sesame Oil and a combination of all-natural Chinese Herbs

Keep Out Of Reach Of Children.

If swallowed, call poison control or seek medical help.

Consulting A Doctor Before Using

On deep or puncture wounds, animal bites or serious burns.

Stop Use And Ask A Doctor

If your condition worsens, does not improve, persists for more than 7 days, or occurs again after a few days.

Purpose

Skin Protectant

Other Information

Store at room temperature. may stain fabrics

Directions

Wash with mild skin cleanser. Pat dry or allow to air dry. Apply an ample amount of ointment over affected skin. Cover with a clean bandage. Repeat procedure every 12 hours until skin improves or as directed by a doctor.

When Using This Product

Do not get into eyes

Warnings

For external use only,When using this product do not get into eyes

* Please review the disclaimer below.

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