NDC 48951-2114 Betula Rhus Special Order
Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 48951 - Uriel Pharmacy Inc.
- 48951-2114 - Betula Rhus Special Order
Product Packages
NDC Code 48951-2114-5
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 48951-2114?
What are the uses for Betula Rhus Special Order?
What are Betula Rhus Special Order Active Ingredients?
- BENZOIC ACID 3 [hp_X]/g - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
- BERBERIS VULGARIS ROOT BARK 4 [hp_X]/g
- BETULA PUBESCENS BARK 2 [hp_X]/g
- COLCHICUM AUTUMNALE WHOLE 5 [hp_X]/g
- FILIPENDULA ULMARIA ROOT 2 [hp_X]/g
- FORMICA RUFA 10 [hp_X]/g
- SAGE 2 [hp_X]/g
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/g
- URTICA URENS 2 [hp_X]/g
Which are Betula Rhus Special Order UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETULA PUBESCENS BARK (UNII: 3R504894L9)
- BETULA PUBESCENS BARK (UNII: 3R504894L9) (Active Moiety)
- SAGE (UNII: 065C5D077J)
- SAGE (UNII: 065C5D077J) (Active Moiety)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS)
- FILIPENDULA ULMARIA ROOT (UNII: 997724QNDS) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- BENZOIC ACID (UNII: 8SKN0B0MIM) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- COLCHICUM AUTUMNALE WHOLE (UNII: W79255C628)
- COLCHICUM AUTUMNALE WHOLE (UNII: W79255C628) (Active Moiety)
- FORMICA RUFA (UNII: 55H0W83JO5)
- FORMICA RUFA (UNII: 55H0W83JO5) (Active Moiety)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
- TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
Which are Betula Rhus 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)
Which are the Pharmacologic Classes for Betula Rhus Special Order?
- Allergens - [CS]
- Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".