73086-201 NDC - LUNATAL DHA (ASCORBIC ACID,CHOLECALCIFEROL,.ALPHA.-TOCOPHEROL ACETATE,DL-,PYRIDOXINE HYDROCHLORIDE,LEVOMEFOLATE CALCIUM,FOLIC ACID,CYANOCOBALAMIN,BIOTIN,CALCIUM CARBONATE,IRON,POTASSIUM IODIDE,MAGNESIUM OXIDE,FISH OIL)

Drug Information

  • Product NDC: 73086-201
  • Proprietary Name: LuNatal DHA
  • Non Proprietary Name: ascorbic acid,cholecalciferol,.alpha.-tocopherol acetate,dl-,pyridoxine hydrochloride,levomefolate calcium,folic acid,cyanocobalamin,biotin,calcium carbonate,iron,potassium iodide,magnesium oxide,fish oil
  • Active Ingredient(s): 60 mg/1 ASCORBIC ACID; 1000 [iU]/1 CHOLECALCIFEROL; 10 [iU]/1 .ALPHA.-TOCOPHEROL ACETATE, DL-; 26 mg/1 PYRIDOXINE HYDROCHLORIDE; 600 ug/1 LEVOMEFOLATE CALCIUM; 400 ug/1 FOLIC ACID; 13 ug/1 CYANOCOBALAMIN; 280 ug/1 BIOTIN; 80 mg/1 CALCIUM CARBONATE; 18 mg/1 IRON; 150 ug/1 POTASSIUM IODIDE; 25 mg/1 MAGNESIUM OXIDE; 350 mg/1 FISH OIL
  • Administration Route(s): ORAL
  • Dosage Form(s): CAPSULE, GELATIN COATED
  • Pharmacy Class(es): Analogs/Derivatives [Chemical/Ingredient]; Ascorbic Acid [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Folate Analog [EPC]; Folic Acid [CS]; 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]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]; Vitamin B 12 [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B12 [EPC]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]; Vitamin D [CS]; Vitamin D [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Skya Health, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:9/4/2026

Package Information

No. Package Code Package Description Billing Unit
173086-201-3030 CAPSULE, GELATIN COATED in 1 BOTTLE (73086-201-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73086-201The 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 PRESCRIPTION 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 NAMELuNatal DHAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEascorbic acid,cholecalciferol,.alpha.-tocopherol acetate,dl-,pyridoxine hydrochloride,levomefolate calcium,folic acid,cyanocobalamin,biotin,calcium carbonate,iron,potassium iodide,magnesium oxide,fish oilThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMECAPSULE, GELATIN COATEDThe 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 DATE9/4/2026This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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 NAMESkya Health, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, DL-; PYRIDOXINE HYDROCHLORIDE; LEVOMEFOLATE CALCIUM; FOLIC ACID; CYANOCOBALAMIN; BIOTIN; CALCIUM CARBONATE; IRON; POTASSIUM IODIDE; MAGNESIUM OXIDE; FISH OILAn 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 STRENGTH60; 1000; 10; 26; 600; 400; 13; 280; 80; 18; 150; 25; 350 
ACTIVE INGRED UNITmg/1; [iU]/1; [iU]/1; mg/1; ug/1; ug/1; ug/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1 
PHARM CLASSESAnalogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Folate Analog [EPC], Folic Acid [CS], 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], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC] 

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This page was last updated on: 10/9/2026

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