66096-153 NDC - OHM PANCREAS AID (HELONIAS DIOICA, LACTICUM ACIDUM, PANCREAS SUIS, PANCREATINUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SYZYGIUM JAMBOLANUM, THYROIDINUM, URANIUM NITRICUM.)

Drug Information

Product NDC: 66096-153

Proprietary Name: OHM Pancreas Aid

Non Proprietary Name: Helonias Dioica, Lacticum Acidum, Pancreas Suis, Pancreatinum, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, Thyroidinum, Uranium Nitricum.

Active Ingredient(s):
  • 30 [hp_C]/59mL CHAMAELIRIUM LUTEUM ROOT;
  • 4 [hp_X]/59mL LACTIC ACID, DL-;
  • 14 [hp_X]/59mL PANCRELIPASE;
  • 10 [hp_X]/59mL PHOSPHORIC ACID;
  • 10 [hp_X]/59mL PHOSPHORUS;
  • 8 [hp_X]/59mL SUS SCROFA PANCREAS;
  • 3 [hp_X]/59mL SYZYGIUM CUMINI SEED;
  • 8 [hp_X]/59mL THYROID, UNSPECIFIED;
  • 12 [hp_X]/59mL URANYL NITRATE HEXAHYDRATE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: OHM PHARMA INC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/3/2015

Package Information

No. Package Code Package Description Billing Unit
166096-153-0559 mL in 1 BOTTLE, SPRAY (66096-153-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC66096-153The 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 NAMEOHM Pancreas AidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEHelonias Dioica, Lacticum Acidum, Pancreas Suis, Pancreatinum, Phosphoricum Acidum, Phosphorus, Syzygium Jambolanum, Thyroidinum, Uranium Nitricum.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE8/3/2015This 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 NAMEOHM PHARMA INC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECHAMAELIRIUM LUTEUM ROOT; LACTIC ACID, DL-; PANCRELIPASE; PHOSPHORIC ACID; PHOSPHORUS; SUS SCROFA PANCREAS; SYZYGIUM CUMINI SEED; THYROID, UNSPECIFIED; URANYL NITRATE HEXAHYDRATEAn 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 STRENGTH30; 4; 14; 10; 10; 8; 3; 8; 12 
ACTIVE INGRED UNIT[hp_C]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 

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