NDC 72290-0001 Df-2

  1. Labeler Index
  2. Agricultural Corporation Health&happy Co.,ltd.
  3. NDC: 72290-0001 Df-2

NDC Product Code 72290-0001

NDC CODE: 72290-0001

Proprietary Name: Df-2 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.

NDC Code Structure

  • 72290 - Agricultural Corporation Health&happy Co.,ltd.

NDC 72290-0001-1

Package Description: 40 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Df-2 with NDC 72290-0001 is a product labeled by Agricultural Corporation Health&happy Co.,ltd.. The product's dosage form is and is administered via form.

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)
  • ADENOSINE (UNII: K72T3FS567)
  • NIACINAMIDE (UNII: 25X51I8RD4)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Agricultural Corporation Health&happy Co.,ltd.
Labeler Code: 72290
Start Marketing Date: 04-01-2018 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Df-2 Product Label Images

Df-2 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

Glycerin

Inactive Ingredient

Water, Niacinamide, Adenosine, etc.

Otc - Purpose

Skin protectant

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

Apply proper amount to the skin.

Warnings

1. Do not use in the following cases(Eczema and scalp wounds)




2.Side Effects




1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor




3.General Precautions




1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately




2)This product is for exeternal use only. Do not use for internal use




4.Storage and handling precautions




1)If possible, avoid direct sunlight and store in cool and area of low humidity




2)In order to maintain the quality of the product and avoid misuse




3)Avoid placing the product near fire and store out in reach of children

Dosage & Administration

For external use only

* Please review the disclaimer below.