NDC 73140-0002 Ddsgen

Camphor, Menthol

NDC Product Code 73140-0002

NDC 73140-0002-1

Package Description: 100 g in 1 PACKAGE

NDC Product Information

Ddsgen with NDC 73140-0002 is a a human over the counter drug product labeled by The Times Co., Ltd.. The generic name of Ddsgen is camphor, menthol. The product's dosage form is cream and is administered via topical form.

Labeler Name: The Times Co., Ltd.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 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.

Ddsgen 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.

  • MENTHOL 1 g/100g
  • CAMPHOR (NATURAL) 1 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.

  • ANGELICA GIGAS ROOT OIL (UNII: 3EYY3K7TBB)

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: The Times Co., Ltd.
Labeler Code: 73140
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: 05-11-2019 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.

Ddsgen Product Label Images

Ddsgen 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

Otc - Active Ingredient

Camphor, menthol

Inactive Ingredient

Ledum palustre extract, ginger extract, angelica gigas extract, etc

Otc - Purpose

Temporary relief of minor aches and pains of muscles and joints

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Apply it on body parts, for arms or legs, apply it on both sides together, and you can have better thermo-therapeutical effect

Warnings

Do not use if you have red rash, swell, itch, or any other abnormal physical symptoms while applying it on your body partsdo not use it on injured body parts, eczema, or dermatitiskeep it at a room temperature and out of children's reachbe careful not to get it in your eyes

Dosage & Administration

For external use only

* Please review the disclaimer below.

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73140-0001
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