NDC 58975-022 Yinchiao
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 58975-022-01
Package Description: 120 TABLET, FILM COATED in 1 BOX
Product Details
What is NDC 58975-022?
What are the uses for Yinchiao?
Which are Yinchiao UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
Which are Yinchiao 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:
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- PLATYCODON GRANDIFLORUM LEAF (UNII: 2L64H2X8DY)
- ARCTIUM LAPPA FRUIT (UNII: EA541308MV)
- MINT (UNII: FV98Z8GITP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SOYBEAN (UNII: L7HT8F1ZOD)
- FORSYTHIA SUSPENSA FRUIT (UNII: P4793M1ES5)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- HYPROMELLOSE 2910 (15000 MPA.S) (UNII: 288VBX44JC)
- GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K)
- NOTOPTERYGIUM INCISUM ROOT (UNII: 5Z2WW4J6RI)
- PHRAGMITES AUSTRALIS ROOT (UNII: BBJ7AOM815)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL 4000 (UNII: 4R4HFI6D95)
- SCHIZONEPETA TENUFOLIA SPIKE (UNII: 2FN3BA1MZE)
What is the NDC to RxNorm Crosswalk for Yinchiao?
- RxCUI: 1091008 - acetaminophen 163 MG / chlorpheniramine maleate 1 MG Oral Tablet
- RxCUI: 1091008 - acetaminophen 162.5 MG / chlorpheniramine maleate 1 MG Oral Tablet
- RxCUI: 1091008 - APAP 163 MG / Chlorpheniramine Maleate 1 MG Oral Tablet
* 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".