NDC 76173-1008 Suyan Jeongdan
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 76173-1008?
What are the uses for Suyan Jeongdan?
Which are Suyan Jeongdan UNII Codes?
The UNII codes for the active ingredients in this product are:
- TEA TREE OIL (UNII: VIF565UC2G)
- TEA TREE OIL (UNII: VIF565UC2G) (Active Moiety)
Which are Suyan Jeongdan 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:
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CLOVE (UNII: K48IKT5321)
- IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O)
- TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)
- BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)
- JOJOBA OIL (UNII: 724GKU717M)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TOCOPHEROL (UNII: R0ZB2556P8)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- AMPELOPSIS JAPONICA ROOT (UNII: O2672197TF)
- ACORUS GRAMINEUS ROOT (UNII: Z60N6Q6E19)
- PRUNUS ARMENIACA SEED (UNII: 75356789IW)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- GINKGO (UNII: 19FUJ2C58T)
- MUNG BEAN (UNII: 1LIB31N73G)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
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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".