NDC 55714-2540 Vitiligo
Echinacea,Iris Versicolor,Rumex Crispus,Berberis Vulgaris,Bovista,Dolichos Pruriens,Hura - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55714 - Newton Laboratories, Inc.
- 55714-2540 - Vitiligo
Product Packages
NDC Code 55714-2540-2
Package Description: 50 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 55714-2540?
What are the uses for Vitiligo?
What are Vitiligo Active Ingredients?
- ARSENIC TRIOXIDE 15 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- BERBERIS VULGARIS ROOT BARK 10 [hp_X]/mL
- CENTELLA ASIATICA 10 [hp_X]/mL - 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.
- DAPHNE MEZEREUM BARK 10 [hp_X]/mL
- ECHINACEA, UNSPECIFIED 10 [hp_X]/mL
- HURA CREPITANS SAP 10 [hp_X]/mL
- IRIS VERSICOLOR ROOT 6 [hp_X]/mL
- LYCOPERDON UTRIFORME FRUITING BODY 10 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 10 [hp_X]/mL
- MUCUNA PRURIENS FRUIT TRICHOME 10 [hp_X]/mL
- RUMEX CRISPUS ROOT 10 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 10 [hp_X]/mL
- TARAXACUM OFFICINALE 10 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
- THUJA OCCIDENTALIS LEAFY TWIG 10 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/mL
- URTICA URENS 10 [hp_X]/mL
Which are Vitiligo UNII Codes?
The UNII codes for the active ingredients in this product are:
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC)
- IRIS VERSICOLOR ROOT (UNII: X43D4L3DQC) (Active Moiety)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F)
- LYCOPERDON UTRIFORME FRUITING BODY (UNII: K2A74U428F) (Active Moiety)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C)
- MUCUNA PRURIENS FRUIT TRICHOME (UNII: 3E271BSI0C) (Active Moiety)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX) (Active Moiety)
- HURA CREPITANS SAP (UNII: 8UHN1I06UP)
- HURA CREPITANS SAP (UNII: 8UHN1I06UP) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (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)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C)
- RUMEX CRISPUS ROOT (UNII: 9N1RM2S62C) (Active Moiety)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
- SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
- TARAXACUM OFFICINALE (UNII: 39981FM375)
- TARAXACUM OFFICINALE (UNII: 39981FM375) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- URTICA URENS (UNII: IHN2NQ5OF9)
- URTICA URENS (UNII: IHN2NQ5OF9) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
Which are Vitiligo 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.
[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".