PRODUCT NDC | 17089-450 | The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
PRODUCT TYPE NAME | HUMAN OTC DRUG | 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. |
PROPRIETARY NAME | GUNA-CELL | The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes. |
NON PROPRIETARY NAME | acetylcarnitine, l-ampc-alpha-lipoic ac-a-tocopherol-ascorbic acid-calc carb-citric ac-cobalamin-colchicum-conium-cupric sulf-herring sperm dna-ferrous fumarate-folic acid-fumaric acid-kali aspartate-mang phos-mang gluconate-mang phos ii-pyruvaldehyde-nat oxalaceticum-sodium pyruvate-niacin-pantothenic acid-ph-podophyllum peltatum-pyridoxine hydrochloride-riboflavin-saccharomyces cerevisiae rna-selenomethionine-succinic acid-sulfur-thiamine hydrochloride-zinc | The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product. |
DOSAGE FORM NAME | SOLUTION/ DROPS | The translation of the dosage form Code submitted by the firm. |
ROUTE NAME | ORAL | The translation of the route code submitted by the firm, indicating route of administration. |
START MARKETING DATE | 5/27/2010 | This is the date that the labeler indicates was the start of its marketing of the drug product. |
MARKETING CATEGORY NAME | UNAPPROVED HOMEOPATHIC | 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. |
LABELER NAME | Guna spa | Name of Company corresponding to the labeler code segment of the Product NDC. |
SUBSTANCE NAME | .ALPHA.-LIPOIC ACID; .ALPHA.-TOCOPHEROL ACETATE, DL-; ACETYLCARNITINE; ADENOSINE CYCLIC PHOSPHATE; ASCORBIC ACID; CALCIUM CARBONATE; CITRIC ACID MONOHYDRATE; COBALAMIN; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; CUPRIC SULFATE; FERROUS FUMARATE; FOLIC ACID; FUMARIC ACID; HERRING SPERM DNA; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; MANGANESE GLUCONATE; MANGANESE PHOSPHATE, DIBASIC; NIACIN; PANTOTHENIC ACID; PHOSPHORUS; PODOPHYLLUM PELTATUM ROOT; POTASSIUM ASPARTATE; PYRIDOXINE HYDROCHLORIDE; PYRUVALDEHYDE; RIBOFLAVIN; SACCHAROMYCES CEREVISIAE RNA; SELENOMETHIONINE; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; SUCCINIC ACID; SULFUR; THIAMINE HYDROCHLORIDE; ZINC | 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. |
ACTIVE NUMERATOR STRENGTH | 3; 3; 3; 6; 3; 3; 3; 3; 6; 6; 3; 3; 3; 3; 6; 3; 3; 6; 3; 3; 4; 6; 3; 6; 10; 6; 6; 3; 3; 3; 3; 3; 4; 3 | |
ACTIVE INGRED UNIT | [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL | |
PHARM CLASSES | Acidifying Activity [MoA], Analogs/Derivatives [Chemical/Ingredient], Anti-coagulant [EPC], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium Chelating Activity [MoA], Calcium [CS], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Carnitine Analog [EPC], Carnitine [CS], Cations, Divalent [CS], Decreased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Nicotinic Acid [EPC], Nicotinic Acids [CS], Osmotic Activity [MoA], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Paramagnetic Contrast Agent [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC] | |