NDC 70931-0003 D-one By Tamdoan Bb Medium

Titanium Dioxide, Zinc Oxide, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Octocrylene, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Adenosine, Arbutin

NDC Product Code 70931-0003

NDC CODE: 70931-0003

Proprietary Name: D-one By Tamdoan Bb Medium 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: Titanium Dioxide, Zinc Oxide, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Octocrylene, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Adenosine, Arbutin 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.
  • Drug uses not available

NDC Code Structure

  • 70931 - Dran Co.,ltd

NDC 70931-0003-1

Package Description: 40 g in 1 TUBE

NDC Product Information

D-one By Tamdoan Bb Medium with NDC 70931-0003 is a a human over the counter drug product labeled by Dran Co.,ltd. The generic name of D-one By Tamdoan Bb Medium is titanium dioxide, zinc oxide, diethylamino hydroxybenzoyl hexyl benzoate, octocrylene, ethylhexyl methoxycinnamate, ethylhexyl salicylate, adenosine, arbutin. The product's dosage form is cream and is administered via topical form.

Labeler Name: Dran 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.

D-one By Tamdoan Bb Medium 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.

  • TITANIUM DIOXIDE 2.54 g/100g
  • ZINC OXIDE 5.99 g/100g
  • DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE 2 g/100g
  • OCTOCRYLENE 1 g/100g
  • OCTINOXATE 7 g/100g
  • OCTISALATE 5 g/100g
  • ADENOSINE .04 g/100g
  • ARBUTIN 2 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.

  • WATER (UNII: 059QF0KO0R)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • ALLANTOIN (UNII: 344S277G0Z)

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: Dran Co.,ltd
Labeler Code: 70931
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: 11-19-2019 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.

D-one By Tamdoan Bb Medium Product Label Images

D-one By Tamdoan Bb Medium 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

Titanium dioxide, Zinc Oxide, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Octocrylene, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Adenosine, Arbutin

Inactive Ingredient

Water, Butylene Glycol, Allantoin, Etc.

Otc - Purpose

  • Helps prevent sunburnProvides high protection from sunburnHelps keep moisturize

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

  • Use as foundation after basic skin care routine or right afternoon when needed (can use before and after makeup)Apply by pressing the puff into the moistened sponge and patting the puff onto the face

Warnings

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

2.Side Effects

1)Due to the use of this product, if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your pharmacist 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.