NDC 62185-0057 Sugar Cravings
Cinnamic Acid,Phloridzinum,Argentum Nitricum,Adenosinum Triphosphoricum Dinatrum,Beet - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62185 - Dr. Donna Restivo Dc
- 62185-0057 - Sugar Cravings
Product Packages
NDC Code 62185-0057-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 62185-0057?
What are the uses for Sugar Cravings?
What are Sugar Cravings Active Ingredients?
- ACER SACCHARUM SAP 6 [hp_C]/mL
- ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_C]/mL
- CINNAMIC ACID 6 [hp_X]/mL
- CORTICOTROPIN 16 [hp_C]/mL
- DEXTROSE 6 [hp_C]/mL
- FRUCTOSE 6 [hp_C]/mL - A monosaccharide in sweet fruits and honey that is soluble in water, alcohol, or ether. It is used as a preservative and an intravenous infusion in parenteral feeding.
- LACTIC ACID, L- 6 [hp_C]/mL
- LACTOSE, UNSPECIFIED FORM 6 [hp_C]/mL
- LYCOPODIUM CLAVATUM SPORE 6 [hp_C]/mL
- MALVIN 15 [hp_C]/mL
- PHLORIZIN 30 [hp_X]/mL
- RIBOSE, D- 6 [hp_C]/mL
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
- SHIGELLA DYSENTERIAE 30 [hp_C]/mL - A species of gram-negative, facultatively anaerobic, rod-shaped bacteria that is extremely pathogenic and causes severe dysentery. Infection with this organism often leads to ulceration of the intestinal epithelium.
- SILVER NITRATE 6 [hp_C]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
- SUCROSE 6 [hp_C]/mL - A nonreducing disaccharide composed of GLUCOSE and FRUCTOSE linked via their anomeric carbons. It is obtained commercially from SUGARCANE, sugar beet (BETA VULGARIS), and other plants and used extensively as a food and a sweetener.
Which are Sugar Cravings UNII Codes?
The UNII codes for the active ingredients in this product are:
- CINNAMIC ACID (UNII: U14A832J8D)
- CINNAMIC ACID (UNII: U14A832J8D) (Active Moiety)
- PHLORIZIN (UNII: CU9S17279X)
- PHLORIZIN (UNII: CU9S17279X) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- SUCROSE (UNII: C151H8M554)
- SUCROSE (UNII: C151H8M554) (Active Moiety)
- DEXTROSE (UNII: IY9XDZ35W2)
- DEXTROSE (UNII: IY9XDZ35W2) (Active Moiety)
- RIBOSE, D- (UNII: 681HV46001)
- RIBOSE, D- (UNII: 681HV46001) (Active Moiety)
- FRUCTOSE (UNII: 6YSS42VSEV)
- FRUCTOSE (UNII: 6YSS42VSEV) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- ACER SACCHARUM SAP (UNII: 75UOH57984)
- ACER SACCHARUM SAP (UNII: 75UOH57984) (Active Moiety)
- LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- MALVIN (UNII: I9I120531L)
- MALVIN (UNII: I9I120531L) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J)
- SHIGELLA DYSENTERIAE (UNII: 1EP6R5562J) (Active Moiety)
- SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4)
- SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS (UNII: Y3V16D4PV4) (Active Moiety)
Which are Sugar Cravings 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)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Sugar Cravings?
* 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".