NDC 67473-103 Sheng Chun Herbal Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67473-103
Proprietary Name:
Sheng Chun Herbal Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sheng Chun Tang Pharmaceutical Industrial Co., Ltd
Labeler Code:
67473
Start Marketing Date: [9]
11-01-2005
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 67473-103-01

Package Description: 3 PATCH in 1 BOX / 4 g in 1 PATCH

Product Details

What is NDC 67473-103?

The NDC code 67473-103 is assigned by the FDA to the product Sheng Chun Herbal Pain Relieving which is product labeled by Sheng Chun Tang Pharmaceutical Industrial Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67473-103-01 3 patch in 1 box / 4 g in 1 patch. 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 Sheng Chun Herbal Pain Relieving?

Adults and children 12 years of age and older: clean and dry affected area. Remove patch from the protective layer, apply to the affected area, rub the area with your hand to secure the patch.Patch will remain effective for 8 hours.Avoid using the same patch on the same area for more than 2 days.Do not apply to area with excessive hair. Adhesive patch may hurt skin upon removal.Wet patch with warm water before removing from skin.Children under 12 years of age: Do not use or consult a doctor.

Which are Sheng Chun Herbal Pain Relieving UNII Codes?

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

Which are Sheng Chun Herbal Pain Relieving 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:

What is the NDC to RxNorm Crosswalk for Sheng Chun Herbal Pain Relieving?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1483688 - menthol 5 % / methyl salicylate 1 % Medicated Patch
  • RxCUI: 1483688 - menthol 0.05 MG/MG / methyl salicylate 0.01 MG/MG Medicated Patch

* 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".