NDC 48951-8265 Rhus Aconitum Special Order
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy Inc.
- 48951-8265 - Rhus Aconitum Special Order
Product Packages
NDC Code 48951-8265-5
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 48951-8265?
What are the uses for Rhus Aconitum Special Order?
Which are Rhus Aconitum Special Order UNII Codes?
The UNII codes for the active ingredients in this product are:
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57)
- PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB)
- MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
- PENOXSULAM (UNII: 784ELC1SCZ)
- PENOXSULAM (UNII: 784ELC1SCZ) (Active Moiety)
Which are Rhus Aconitum Special Order 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)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- FRANKINCENSE OIL (UNII: 67ZYA5T02K)
- MYRRH OIL (UNII: H74221J5J4)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
* 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".