NDC 63083-2021 Epstein Barr Drops 2021
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-2021?
What are the uses for Epstein Barr Drops 2021?
Which are Epstein Barr Drops 2021 UNII Codes?
The UNII codes for the active ingredients in this product are:
- BOS TAURUS BONE MARROW (UNII: 08X0K2M57P)
- BOS TAURUS BONE MARROW (UNII: 08X0K2M57P) (Active Moiety)
- CAUSTICUM (UNII: DD5FO1WKFU)
- CAUSTICUM (UNII: DD5FO1WKFU) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE)
- HYSSOPUS OFFICINALIS WHOLE (UNII: 0IQW001KPE) (Active Moiety)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX)
- HUMAN HERPESVIRUS 4 (UNII: 2A26YW7PNX) (Active Moiety)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I)
- HAEMOPHILUS INFLUENZAE (UNII: K738E2MB3I) (Active Moiety)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR)
- STREPTOCOCCUS VIRIDANS GROUP (UNII: NNV2379HKR) (Active Moiety)
- TOXOPLASMA GONDII (UNII: BMV90JF469)
- TOXOPLASMA GONDII (UNII: BMV90JF469) (Active Moiety)
Which are Epstein Barr Drops 2021 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".