NDC 72932-004 Zonsen Sting Relief Pad

Isopropyl Alcohol, Benzocaine

NDC Product Code 72932-004

NDC 72932-004-00

Package Description: 1 PACKET in 1 POUCH > .4 mL in 1 PACKET

NDC Product Information

Zonsen Sting Relief Pad with NDC 72932-004 is a a human over the counter drug product labeled by Wuhan Zonsen Medical Products Co., Ltd.. The generic name of Zonsen Sting Relief Pad is isopropyl alcohol, benzocaine. The product's dosage form is swab and is administered via topical form.

Labeler Name: Wuhan Zonsen Medical Products Co., Ltd.

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab 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.

Zonsen Sting Relief Pad 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.

  • ISOPROPYL ALCOHOL .7 mL/mL
  • BENZOCAINE 60 mg/mL

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: Wuhan Zonsen Medical Products Co., Ltd.
Labeler Code: 72932
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: 04-01-2019 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.

Zonsen Sting Relief Pad Product Label Images

Zonsen Sting Relief Pad 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

Isopropyl Alcohol 70%Benzocaine 6%

Purpose

AntisepticTopical Analgesic

Use

For prevent infection in minor scrape and temporary relief of itching of insect bites

Warnings

  • For external use only.Flammable, keep away from fire or flame.

Do Not Use

  • With electrocautery procedures.In the eyes. If contact occurs, flush eyes with water.

Stop Use

If irritation and redness develop. If condition continues, consult your health care practitioner.

Keep Out Of Reach Of Children.

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

Directions

  • Apply to affected area 3 or 4 times daily.For adults and children 2 years of age and older.Children under 2 years :consult physician.

Other Information

Store at room temperature 15°C-30°C(59°F-86°F)

Inactive Ingredients:

Purified water

* Please review the disclaimer below.

Previous Code
72932-003
Next Code
72933-000