NDC 76173-1005 Suyan Chungsoo
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 76173-1005?
What are the uses for Suyan Chungsoo?
Which are Suyan Chungsoo UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARBUTIN (UNII: C5INA23HXF)
- ARBUTIN (UNII: C5INA23HXF) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Suyan Chungsoo 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)
- ALCOHOL (UNII: 3K9958V90M)
- BETAINE (UNII: 3SCV180C9W)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
- BLETILLA STRIATA BULB (UNII: 00T5SH6SEJ)
- CLOVE (UNII: K48IKT5321)
- IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O)
- MUNG BEAN (UNII: 1LIB31N73G)
- FU LING (UNII: XH37TWY5O4)
- TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- PANTHENOL (UNII: WV9CM0O67Z)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- XANTHAN GUM (UNII: TTV12P4NEE)
- RAFFINOSE (UNII: N5O3QU595M)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CERAMIDE 3 (UNII: 4370DF050B)
- YEAST (UNII: 3NY3SM6B8U)
- TROLAMINE (UNII: 9O3K93S3TK)
- SOY PROTEIN (UNII: R44IWB3RN5)
- RICE BRAN (UNII: R60QEP13IC)
* Please review the disclaimer below.
[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".