NDC 63083-2023 Facial Pain Drops 2023
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2023?
What are the uses for Facial Pain Drops 2023?
Which are Facial Pain Drops 2023 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALIX ALBA BARK (UNII: 205MXS71H7)
- SALIX ALBA BARK (UNII: 205MXS71H7) (Active Moiety)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN)
- AMARYLLIS BELLADONNA WHOLE (UNII: 11B89M58UN) (Active Moiety)
- BOS TAURUS NERVE (UNII: 28G2U3MQJK)
- BOS TAURUS NERVE (UNII: 28G2U3MQJK) (Active Moiety)
Which are Facial Pain Drops 2023 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
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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".