NDC 75932-1002 Morisu
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 75932-1002?
What are the uses for Morisu?
Which are Morisu UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYALURONIC ACID (UNII: S270N0TRQY)
- HYALURONIC ACID (UNII: S270N0TRQY) (Active Moiety)
Which are Morisu 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:
- ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU)
- CANANGA OIL (UNII: 8YOY78GNNX)
- LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P)
- GLYCERIN (UNII: PDC6A3C0OX)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WATER (UNII: 059QF0KO0R)
- ADENOSINE (UNII: K72T3FS567)
- SESAME OIL (UNII: QX10HYY4QV)
- ARTEMISIA PRINCEPS LEAF (UNII: SY077EW02G)
- HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)
- TEA LEAF (UNII: GH42T47V24)
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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".