NDC 81799-009 Shingles Pain Relief Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81799 - Ehy Holdings Llc
- 81799-009 - Shingles Pain Relief Cream
Product Packages
NDC Code 81799-009-01
Package Description: 60 g in 1 BOTTLE
Product Details
What is NDC 81799-009?
What are the uses for Shingles Pain Relief Cream?
Which are Shingles Pain Relief Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- WORMWOOD (UNII: F84709P2XV)
- WORMWOOD (UNII: F84709P2XV) (Active Moiety)
Which are Shingles Pain Relief Cream 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:
- DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
- WATER (UNII: 059QF0KO0R)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- SMILAX GLABRA WHOLE (UNII: H51N91QNEB)
- CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
- BASSIA SCOPARIA POLLEN (UNII: 07A108ZKW5)
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[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".