NDC 61658-001 Yunnan Baiyao Arthritis Pain Relief

NDC Product Code 61658-001

NDC CODE: 61658-001

Proprietary Name: Yunnan Baiyao Arthritis Pain Relief 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

  • 61658 - Yunnan Baiyao Group Co., Ltd.
    • 61658-001 - Yunnan Baiyao Arthritis Pain Relief

NDC 61658-001-01

Package Description: 1 POUCH in 1 BOX > 6 PLASTER in 1 POUCH

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

NDC Product Information

Yunnan Baiyao Arthritis Pain Relief with NDC 61658-001 is a product labeled by Yunnan Baiyao Group 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.

  • PEPPERMINT OIL (UNII: AV092KU4JH)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • LANOLIN (UNII: 7EV65EAW6H)
  • ROSIN (UNII: 88S87KL877)
  • ZINC OXIDE (UNII: SOI2LOH54Z)
  • NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)

Product Labeler Information

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

Labeler Name: Yunnan Baiyao Group Co., Ltd.
Labeler Code: 61658
Start Marketing Date: 06-18-2015 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: 12-31-2017 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".

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Yunnan Baiyao Arthritis Pain Relief Product Label Images