NDC 55496-1001 Park No Suk A Clear Walk Of Park
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55496 - Park No Suk A Clear Walk Of Park
- 55496-1001 - Park No Suk A Clear Walk Of Park
Product Packages
NDC Code 55496-1001-1
Package Description: 30 g in 1 BOTTLE
Product Details
What is NDC 55496-1001?
What are the uses for Park No Suk A Clear Walk Of Park?
Which are Park No Suk A Clear Walk Of Park UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN)
- ANGELICA ARCHANGELICA ROOT (UNII: DTN01M69SN) (Active Moiety)
Which are Park No Suk A Clear Walk Of Park 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:
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- FU LING (UNII: XH37TWY5O4)
- IPOMOEA PURPUREA SEED (UNII: SS0Y753VJB)
- TANACETUM CINERARIIFOLIUM FLOWER (UNII: CGF76TP7X6)
- PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- PASSIFLORA INCARNATA SEED (UNII: 4J066IR2BL)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
- TRIPTERYGIUM WILFORDII ROOT (UNII: 06Q6W5UGMZ)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- CHINESE CHESTNUT (UNII: 2774MIM2V7)
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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".