NDC 70931-0005 Wonder Intensive Bbcream 21 (light)

NDC Product Code 70931-0005

NDC 70931-0005-1

Package Description: 40 g in 1 TUBE

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

NDC Product Information

Wonder Intensive Bbcream 21 (light) with NDC 70931-0005 is a product labeled by Dran Co.,ltd. The generic name of Wonder Intensive Bbcream 21 (light) is . The product's dosage form is and is administered via form.

Labeler Name: Dran Co.,ltd

Dosage Form: -

Product Type: 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.

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)

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
Start Marketing Date: 02-23-2016 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: 12-31-2018 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 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.

Wonder Intensive Bbcream 21 (light) Product Label Images

Wonder Intensive Bbcream 21 (light) 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.