62185-0056 NDC - WLP40 (ASCLEPIAS VINCETOXICUM, ECHINACEA (ANGUSTIFOLIA), HYPOTHALAMUS (SUIS), CEREBRUM SUIS, HEPAR SUIS, KIDNEY SUIS, METHYLCOBALAMIN, PANCREAS SUIS, STOMACH (SUIS), AACG-A, AACG-B, CALCAREA CARBONICA, GELSEMIUM SEMPERVIRENS, GRAPHITES, NUX VOMICA, PHYTOLACCA DECANDRA, GAMBOGIA, 7-OXO-DEHYDROEPIANDROSTERONE-ACETATE (7-KETO), ADENOSINUM TRIPHOSPHORICUM DINATRUM, INSULINUM (SUIS), SARCOLACTICUM ACIDUM, PROTEUS (VULGARIS))

Drug Information

Product NDC: 62185-0056

Proprietary Name: WLP40

Non Proprietary Name: Asclepias Vincetoxicum, Echinacea (Angustifolia), Hypothalamus (Suis), Cerebrum Suis, Hepar Suis, Kidney Suis, Methylcobalamin, Pancreas Suis, Stomach (Suis), AACG-A, AACG-B, Calcarea Carbonica, Gelsemium Sempervirens, Graphites, Nux Vomica, Phytolacca Decandra, Gambogia, 7-oxo-dehydroepiandrosterone-acetate (7-KETO), Adenosinum Triphosphoricum Dinatrum, Insulinum (Suis), Sarcolacticum Acidum, Proteus (Vulgaris)

Active Ingredient(s):
  • 30 [hp_X]/mL 7-OXODEHYDROEPIANDROSTERONE 3-ACETATE;
  • 30 [hp_X]/mL ADENOSINE TRIPHOSPHATE DISODIUM;
  • 8 [hp_X]/mL APC-356433;
  • 8 [hp_X]/mL APC-356434;
  • 6 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE;
  • 14 [hp_X]/mL GAMBOGE;
  • 12 [hp_X]/mL GELSEMIUM SEMPERVIRENS ROOT;
  • 12 [hp_X]/mL GRAPHITE;
  • 30 [hp_X]/mL INSULIN PORK;
  • 30 [hp_X]/mL LACTIC ACID, L-;
  • 8 [hp_X]/mL METHYLCOBALAMIN;
  • 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 8 [hp_X]/mL PORK KIDNEY;
  • 8 [hp_X]/mL PORK LIVER;
  • 30 [hp_C]/mL PROTEUS VULGARIS;
  • 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED;
  • 8 [hp_X]/mL SUS SCROFA CEREBRUM;
  • 6 [hp_X]/mL SUS SCROFA HYPOTHALAMUS;
  • 8 [hp_X]/mL SUS SCROFA PANCREAS;
  • 8 [hp_X]/mL SUS SCROFA STOMACH;
  • 6 [hp_X]/mL VINCETOXICUM HIRUNDINARIA ROOT


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS]

Labeler Information

Labeler Name: Dr. Donna Restivo DC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/23/2020

Package Information

No. Package Code Package Description Billing Unit
162185-0056-130 mL in 1 BOTTLE, DROPPER (62185-0056-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62185-0056The 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 NAMEWLP40The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAsclepias Vincetoxicum, Echinacea (Angustifolia), Hypothalamus (Suis), Cerebrum Suis, Hepar Suis, Kidney Suis, Methylcobalamin, Pancreas Suis, Stomach (Suis), AACG-A, AACG-B, Calcarea Carbonica, Gelsemium Sempervirens, Graphites, Nux Vomica, Phytolacca Decandra, Gambogia, 7-oxo-dehydroepiandrosterone-acetate (7-KETO), Adenosinum Triphosphoricum Dinatrum, Insulinum (Suis), Sarcolacticum Acidum, Proteus (Vulgaris)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 DATE3/23/2020This 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 NAMEDr. Donna Restivo DCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME7-OXODEHYDROEPIANDROSTERONE 3-ACETATE; ADENOSINE TRIPHOSPHATE DISODIUM; APC-356433; APC-356434; ECHINACEA ANGUSTIFOLIA WHOLE; GAMBOGE; GELSEMIUM SEMPERVIRENS ROOT; GRAPHITE; INSULIN PORK; LACTIC ACID, L-; METHYLCOBALAMIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; PORK KIDNEY; PORK LIVER; PROTEUS VULGARIS; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA CEREBRUM; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PANCREAS; SUS SCROFA STOMACH; VINCETOXICUM HIRUNDINARIA ROOTAn 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; 30; 8; 8; 6; 14; 12; 12; 30; 30; 8; 12; 12; 8; 8; 30; 12; 8; 6; 8; 8; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] 

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