NDC 55502-1001 B.s.c Ampul
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 55502-1001?
What are the uses for B.s.c Ampul?
Which are B.s.c Ampul UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are B.s.c Ampul 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:
- HUMAN ADIPOSE (UNII: LOS728452T)
- PANAX GINSENG WHOLE (UNII: 9L5JEP7MES)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- PREZATIDE (UNII: 39TG2H631E)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALLANTOIN (UNII: 344S277G0Z)
- HEXANEDIOL (UNII: ZIA319275I)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BETAINE (UNII: 3SCV180C9W)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- ARBUTIN (UNII: C5INA23HXF)
- SNAIL, UNSPECIFIED (UNII: 2VIO5GL90I)
- THUJOPSIS DOLABRATA WHOLE (UNII: Q190548W6J)
- MAGNOLIA KOBUS BARK (UNII: 54LVP49595)
- PUMMELO (UNII: ET1TN5W71X)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- TEA LEAF OIL (UNII: VC855RRT77)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)
- SQUALANE (UNII: GW89575KF9)
- SHEA BUTTER (UNII: K49155WL9Y)
- CERAMIDE 3 (UNII: 4370DF050B)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PEA PROTEIN (UNII: 7Q50F46595)
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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".