NDC 17089-291 Guna-lympho
Apis Mellifera - Calendula Officinalis Flower - Centella Asiatica - - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17089 - Guna Spa
- 17089-291 - Guna-lympho
Product Packages
NDC Code 17089-291-18
Package Description: 1 BOTTLE, DROPPER in 1 BOX / 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 17089-291?
What are the uses for Guna-lympho?
What are Guna-lympho Active Ingredients?
- APIS MELLIFERA 8 [hp_X]/30mL
- CALENDULA OFFICINALIS FLOWER 1 [hp_X]/30mL
- CENTELLA ASIATICA 1 [hp_X]/30mL - A plant of the family APIACEAE which is the source of asiatic acid and asiaticoside. Centella asiatica (L.) Urb. = Hydrocotyle asiatica L. is known for effect on peripheral circulation.
- DODECAHYDROXYCYCLOHEXANE DIHYDRATE 6 [hp_X]/30mL
- EQUISETUM HYEMALE 3 [hp_X]/30mL
- FUMARIC ACID 6 [hp_X]/30mL
- GOLDENSEAL 1 [hp_X]/30mL
- GRAPHITE 30 [hp_X]/30mL - An allotropic form of carbon that is used in pencils, as a lubricant, and in matches and explosives. It is obtained by mining and its dust can cause lung irritation.
- JUGLANS REGIA LEAF 3 [hp_X]/30mL
- LEVOTHYROXINE 12 [hp_X]/30mL
- MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE 6 [hp_X]/30mL
- MALIC ACID 6 [hp_X]/30mL
- MYOSOTIS ARVENSIS 3 [hp_X]/30mL
- PHYTOLACCA AMERICANA ROOT 3 [hp_X]/30mL
- SARSAPARILLA 3 [hp_X]/30mL
- SODIUM DIETHYL OXALACETATE 6 [hp_X]/30mL
- SODIUM PYRUVATE 6 [hp_X]/30mL
- SUS SCROFA CAPILLARY TISSUE 6 [hp_X]/30mL
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE 6 [hp_X]/30mL
- SUS SCROFA VEIN 6 [hp_X]/30mL
- TARAXACUM OFFICINALE 1 [hp_X]/30mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
Which are Guna-lympho UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)
- SUS SCROFA CAPILLARY TISSUE (UNII: 253A0356PN)
- SUS SCROFA CAPILLARY TISSUE (UNII: 253A0356PN) (Active Moiety)
- MALIC ACID (UNII: 817L1N4CKP)
- MALIC ACID (UNII: 817L1N4CKP) (Active Moiety)
- EQUISETUM HYEMALE (UNII: 59677RXH25)
- EQUISETUM HYEMALE (UNII: 59677RXH25) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- GOLDENSEAL (UNII: ZW3Z11D0JV) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- JUGLANS REGIA LEAF (UNII: 85HKB87105)
- JUGLANS REGIA LEAF (UNII: 85HKB87105) (Active Moiety)
- LEVOTHYROXINE (UNII: Q51BO43MG4)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72)
- SUS SCROFA SMALL INTESTINE MUCOSA LYMPH FOLLICLE (UNII: 308LM01C72) (Active Moiety)
- MAGNESIUM PHOSPHATE (UNII: 453COF7817)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J)
- MYOSOTIS ARVENSIS (UNII: C73BK97H5J) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- SODIUM PYRUVATE (UNII: POD38AIF08)
- PYRUVIC ACID (UNII: 8558G7RUTR) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SARSAPARILLA (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- DODECAHYDROXYCYCLOHEXANE DIHYDRATE (UNII: 5BWD2J7B4W)
- DODECAHYDROXYCYCLOHEXANE (UNII: I1Z9VS3H64) (Active Moiety)
- SUS SCROFA VEIN (UNII: 2510RH3I89)
- SUS SCROFA VEIN (UNII: 2510RH3I89) (Active Moiety)
Which are Guna-lympho 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)
Which are the Pharmacologic Classes for Guna-lympho?
- Allergens - [CS]
- Bee Venoms - [CS]
- Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Increased Large Intestinal Motility - [PE] (Physiologic Effect)
- Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
- Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
- Osmotic Activity - [MoA] (Mechanism of Action)
- Osmotic Laxative - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
- Thyroxine - [CS]
- l-Thyroxine - [EPC] (Established Pharmacologic Class)
* 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".