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  4. NDC Product Code: 82672-302 Miraculous

NDC 82672-302 Miraculous

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82672-302?
  4. Miraculous 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:
82672-302
Proprietary Name:
Miraculous
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Qingdao Aolixin Sanitary Products Co., Ltd.
Labeler Code:
82672
Product Label ID:
dce4236f-6c1a-21b6-e053-2995a90a29fa
Start Marketing Date: [9]
04-20-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82672-302?

The NDC code 82672-302 is assigned by the FDA to the product Miraculous which is product labeled by Qingdao Aolixin Sanitary Products Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82672-302-01 9 g in 1 bag . 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 Miraculous?

For those under 60 years old, take one package (9g) three times a day, two hours after breakfast and lunch, and one package (9g) 30 minutes before going to bed It is recommended to eat one package (9g) 2 hours after breakfast and one package (9g) 30 minutes before going to bed.

Which are Miraculous UNII Codes?

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

  • ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
  • ANGELICA SINENSIS ROOT (UNII: B66F4574UG) (Active Moiety)
  • PLATYCODON GRANDIFLORUS ROOT (UNII: 2DF0NS0O2Z)
  • PLATYCODON GRANDIFLORUS ROOT (UNII: 2DF0NS0O2Z) (Active Moiety)

Which are Miraculous 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".