NDC 57955-5116 Poison Ivy And Oak Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-5116 - Poison Ivy And Oak Relief
Product Packages
NDC Code 57955-5116-2
Package Description: 1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-5116?
What are the uses for Poison Ivy And Oak Relief?
Which are Poison Ivy And Oak Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E)
- ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (Active Moiety)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F)
- CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (Active Moiety)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E)
- CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (Active Moiety)
- CYPRIPEDIUM PARVIFOLUM ROOT (UNII: 21Y9GZ1LZA)
- CYPRIPEDIUM PARVIFOLUM ROOT (UNII: 21Y9GZ1LZA) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- ERECHTITES HIERACIIFOLIUS (UNII: 1L6JHK0ORR)
- ERECHTITES HIERACIIFOLIUS (UNII: 1L6JHK0ORR) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- GRINDELIA HIRSUTULA WHOLE (UNII: C08B09D8UJ)
- GRINDELIA HIRSUTULA WHOLE (UNII: C08B09D8UJ) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
Which are Poison Ivy And Oak Relief 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:
- WATER (UNII: 059QF0KO0R)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".