NDC 63083-1013 Poison Ivy/oak 1013
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-1013?
What are the uses for Poison Ivy/oak 1013?
Which are Poison Ivy/oak 1013 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98)
- ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- XEROPHYLLUM ASPHODELOIDES WHOLE (UNII: 9I4XB1GP2B)
- XEROPHYLLUM ASPHODELOIDES WHOLE (UNII: 9I4XB1GP2B) (Active Moiety)
- TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ)
- TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- URTICA DIOICA SUBSP. DIOICA LEAF (UNII: 232L6DS3Y4)
- URTICA DIOICA SUBSP. DIOICA LEAF (UNII: 232L6DS3Y4) (Active Moiety)
- AILANTHUS ALTISSIMA FRUIT (UNII: 0W913N2K5N)
- AILANTHUS ALTISSIMA FRUIT (UNII: 0W913N2K5N) (Active Moiety)
Which are Poison Ivy/oak 1013 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)
* Please review the disclaimer below.
[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".