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  4. NDC Product Code: 70098-0017 Dr.double Ha Ultra Soothing Essence

NDC 70098-0017 Dr.double Ha Ultra Soothing Essence

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70098-0017?
  4. Dr.double Ha Ultra Soothing Essence Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70098-0017
Proprietary Name:
Dr.double Ha Ultra Soothing Essence
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gk Cosmetic Co., Ltd.
Labeler Code:
70098
Product Label ID:
b77f7242-c2e1-414b-e053-2a95a90abb81
Start Marketing Date: [9]
12-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 70098-0017?

The NDC code 70098-0017 is assigned by the FDA to the product Dr.double Ha Ultra Soothing Essence which is product labeled by Gk Cosmetic Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70098-0017-2 50 ml in 1 bottle, spray . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Dr.double Ha Ultra Soothing Essence?

Clean the skin before use, spray an appropriate amount, and massage it to absorb enough. It can be used in all skin areas including the face and scalp.

Which are Dr.double Ha Ultra Soothing Essence UNII Codes?

The UNII codes for the active ingredients in this product are:

  • HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
  • HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) (Active Moiety)
  • PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)
  • PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68) (Active Moiety)

Which are Dr.double Ha Ultra Soothing Essence Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".