17089-450 NDC - GUNA-CELL (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)

Drug Information

Product NDC: 17089-450

Proprietary Name: GUNA-CELL

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

Active Ingredient(s):
  • 3 [hp_X]/30mL .ALPHA.-LIPOIC ACID;
  • 3 [hp_X]/30mL .ALPHA.-TOCOPHEROL ACETATE, DL-;
  • 3 [hp_X]/30mL ACETYLCARNITINE;
  • 6 [hp_X]/30mL ADENOSINE CYCLIC PHOSPHATE;
  • 3 [hp_X]/30mL ASCORBIC ACID;
  • 3 [hp_X]/30mL CALCIUM CARBONATE;
  • 3 [hp_X]/30mL CITRIC ACID MONOHYDRATE;
  • 3 [hp_X]/30mL COBALAMIN;
  • 6 [hp_X]/30mL COLCHICUM AUTUMNALE BULB;
  • 6 [hp_X]/30mL CONIUM MACULATUM FLOWERING TOP;
  • 3 [hp_X]/30mL CUPRIC SULFATE;
  • 3 [hp_X]/30mL FERROUS FUMARATE;
  • 3 [hp_X]/30mL FOLIC ACID;
  • 3 [hp_X]/30mL FUMARIC ACID;
  • 6 [hp_X]/30mL HERRING SPERM DNA;
  • 3 [hp_X]/30mL MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE;
  • 3 [hp_X]/30mL MANGANESE GLUCONATE;
  • 6 [hp_X]/30mL MANGANESE PHOSPHATE, DIBASIC;
  • 3 [hp_X]/30mL NIACIN;
  • 3 [hp_X]/30mL PANTOTHENIC ACID;
  • 4 [hp_X]/30mL PHOSPHORUS;
  • 6 [hp_X]/30mL PODOPHYLLUM PELTATUM ROOT;
  • 3 [hp_X]/30mL POTASSIUM ASPARTATE;
  • 6 [hp_X]/30mL PYRIDOXINE HYDROCHLORIDE;
  • 10 [hp_X]/30mL PYRUVALDEHYDE;
  • 6 [hp_X]/30mL RIBOFLAVIN;
  • 6 [hp_X]/30mL SACCHAROMYCES CEREVISIAE RNA;
  • 3 [hp_X]/30mL SELENOMETHIONINE;
  • 3 [hp_X]/30mL SODIUM DIETHYL OXALACETATE;
  • 3 [hp_X]/30mL SODIUM PYRUVATE;
  • 3 [hp_X]/30mL SUCCINIC ACID;
  • 3 [hp_X]/30mL SULFUR;
  • 4 [hp_X]/30mL THIAMINE HYDROCHLORIDE;
  • 3 [hp_X]/30mL ZINC


Administration Route(s): ORAL

Dosage Form(s): SOLUTION/ DROPS

Pharmacy Class(es):
  • 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]

Labeler Information

Labeler Name: Guna spa
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/27/2010

Package Information

No. Package Code Package Description Billing Unit
117089-450-181 BOTTLE, DROPPER in 1 BOX (17089-450-18) / 30 mL in 1 BOTTLE, DROPPER

NDC Record

Field Name Field Value Definition
PRODUCT NDC17089-450The 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 NAMEHUMAN OTC DRUGIndicates 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 NAMEGUNA-CELLThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEacetylcarnitine, 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-zincThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/27/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEGuna spaName 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; ZINCAn 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 STRENGTH3; 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 CLASSESAcidifying 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] 

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This page was last updated on: 2/1/2023