NDC 50488-2626 Morcin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 50488-2626 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
Product Details
What is NDC 50488-2626?
Which are Morcin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- BELLADONNA LEAF (UNII: 6GZW20TIOI)
- BELLADONNA LEAF (UNII: 6GZW20TIOI) (Active Moiety)
- BELLIS PERENNIS (UNII: 2HU33I03UY)
- BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
- MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- COLCHICUM AUTUMNALE FLOWER (UNII: 097FL89535)
- COLCHICUM AUTUMNALE FLOWER (UNII: 097FL89535) (Active Moiety)
- HAMAMELIS VIRGINIANA WHOLE (UNII: V663Q8TEFU)
- HAMAMELIS VIRGINIANA WHOLE (UNII: V663Q8TEFU) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
- HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
- ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
Which are Morcin 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:
- SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- WATER (UNII: 059QF0KO0R)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)
- SHEA BUTTER (UNII: K49155WL9Y)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHAMOMILE (UNII: FGL3685T2X)
- BLACK COHOSH (UNII: K73E24S6X9)
- CUCUMBER (UNII: YY7C30VXJT)
- TURMERIC (UNII: 856YO1Z64F)
- LICORICE (UNII: 61ZBX54883)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ILEX PARAGUARIENSIS WHOLE (UNII: QJB02841ZY)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- JOJOBA OIL (UNII: 724GKU717M)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- VITAMIN A (UNII: 81G40H8B0T)
- CURDLAN (UNII: 6930DL209R)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".