66096-695 NDC - OHM DRAINAGE LYMPHATIC (AESCULUS HIPP, APIS MEL, ARANEA, BARYTA CARB, EQUISETUM HYEM, FUCUS, FUMARIA, JUGLANS CIN, KALI IOD, KALI MUR, MYOSOTIS, NASTURTIUM, NAT SULPHURICUM, PHYTOLACCA, SARSAPARILLA, SCROPHULARA, SECALE, TEUCRIUM SCOR, THYROIDINUM, VIPERA.)

Drug Information

Product NDC: 66096-695

Proprietary Name: OHM Drainage Lymphatic

Non Proprietary Name: Aesculus Hipp, Apis Mel, Aranea, Baryta Carb, Equisetum Hyem, Fucus, Fumaria, Juglans Cin, Kali Iod, Kali Mur, Myosotis, Nasturtium, Nat Sulphuricum, Phytolacca, Sarsaparilla, Scrophulara, Secale, Teucrium Scor, Thyroidinum, Vipera.

Active Ingredient(s):
  • 4 [hp_X]/100g APIS MELLIFERA;
  • 14 [hp_X]/100g ARANEUS DIADEMATUS;
  • 14 [hp_X]/100g BARIUM CARBONATE;
  • 6 [hp_X]/100g CLAVICEPS PURPUREA SCLEROTIUM;
  • 3 [hp_X]/100g EQUISETUM HYEMALE;
  • 3 [hp_X]/100g FUCUS VESICULOSUS;
  • 2 [hp_X]/100g FUMARIA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/100g HORSE CHESTNUT;
  • 2 [hp_X]/100g JUGLANS CINEREA BRANCH BARK/ROOT BARK;
  • 2 [hp_X]/100g MYOSOTIS ARVENSIS;
  • 2 [hp_X]/100g NASTURTIUM OFFICINALE;
  • 2 [hp_X]/100g PHYTOLACCA AMERICANA ROOT;
  • 2 [hp_X]/100g POTASSIUM CHLORIDE;
  • 2 [hp_X]/100g POTASSIUM IODIDE;
  • 3 [hp_X]/100g SCROPHULARIA NODOSA;
  • 2 [hp_X]/100g SMILAX ORNATA ROOT;
  • 2 [hp_X]/100g SODIUM SULFATE;
  • 2 [hp_X]/100g TEUCRIUM SCORODONIA FLOWERING TOP;
  • 10 [hp_X]/100g THYROID, UNSPECIFIED;
  • 6 [hp_X]/100g VIPERA BERUS VENOM


Administration Route(s): TOPICAL

Dosage Form(s): GEL

Pharmacy Class(es):
  • Allergens [CS];
  • Bee Venoms [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC];
  • Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Labeler Name: OHM PHARMA INC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/16/2014

Package Information

No. Package Code Package Description Billing Unit
166096-695-10100 g in 1 TUBE (66096-695-10)

NDC Record

Field Name Field Value Definition
PRODUCT NDC66096-695The 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 Drainage LymphaticThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAesculus Hipp, Apis Mel, Aranea, Baryta Carb, Equisetum Hyem, Fucus, Fumaria, Juglans Cin, Kali Iod, Kali Mur, Myosotis, Nasturtium, Nat Sulphuricum, Phytolacca, Sarsaparilla, Scrophulara, Secale, Teucrium Scor, Thyroidinum, Vipera.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEGELThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/16/2014This 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 NAMEAPIS MELLIFERA; ARANEUS DIADEMATUS; BARIUM CARBONATE; CLAVICEPS PURPUREA SCLEROTIUM; EQUISETUM HYEMALE; FUCUS VESICULOSUS; FUMARIA OFFICINALIS FLOWERING TOP; HORSE CHESTNUT; JUGLANS CINEREA BRANCH BARK/ROOT BARK; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; POTASSIUM IODIDE; SCROPHULARIA NODOSA; SMILAX ORNATA ROOT; SODIUM SULFATE; TEUCRIUM SCORODONIA FLOWERING TOP; THYROID, UNSPECIFIED; VIPERA BERUS VENOMAn 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 STRENGTH4; 14; 14; 6; 3; 3; 2; 4; 2; 2; 2; 2; 2; 2; 3; 2; 2; 2; 10; 6 
ACTIVE INGRED UNIT[hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g; [hp_X]/100g 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Insect Venom Allergenic Extract [EPC] 

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