66492-038 NDC - LUNG DROPS (BELLADONNA, IPECACUANHA, LOBELIA INFLATA, QUEBRACHO, ANTIMONIUM TARTARICUM, BLATTA ORIENTALIS, NAPHTHALINUM, NATRUM SULPHURICUM, PULSATILLA, RUMEX CRISPUS, MERCURIUS SOLUBILIS, ADRENALINUM.)

Drug Information

Product NDC: 66492-038

Proprietary Name: Lung Drops

Non Proprietary Name: Belladonna, Ipecacuanha, Lobelia Inflata, Quebracho, Antimonium Tartaricum, Blatta Orientalis, Naphthalinum, Natrum Sulphuricum, Pulsatilla, Rumex Crispus, Mercurius Solubilis, Adrenalinum.

Active Ingredient(s):
  • 6 [hp_X]/59mL ANEMONE PULSATILLA;
  • 6 [hp_X]/59mL ANTIMONY POTASSIUM TARTRATE;
  • 5 [hp_X]/59mL ASPIDOSPERMA QUEBRACHO-BLANCO BARK;
  • 4 [hp_X]/59mL ATROPA BELLADONNA;
  • 6 [hp_X]/59mL BLATTA ORIENTALIS;
  • 5 [hp_C]/59mL EPINEPHRINE;
  • 4 [hp_X]/59mL IPECAC;
  • 4 [hp_X]/59mL LOBELIA INFLATA;
  • 8 [hp_X]/59mL MERCURIUS SOLUBILIS;
  • 6 [hp_X]/59mL NAPHTHALENE;
  • 6 [hp_X]/59mL RUMEX CRISPUS ROOT;
  • 6 [hp_X]/59mL SODIUM SULFATE


Administration Route(s): SUBLINGUAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Adrenergic alpha-Agonists [MoA];
  • Adrenergic beta-Agonists [MoA];
  • Allergens [CS];
  • Catecholamine [EPC];
  • Catecholamines [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Insect Proteins [CS];
  • Non-Standardized Insect Allergenic Extract [EPC];
  • alpha-Adrenergic Agonist [EPC];
  • beta-Adrenergic Agonist [EPC]

Labeler Information

Labeler Name: Be Well Medical dba Richard Clement Nutrition y Be Well Homeopathics
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:11/25/2014

Package Information

No. Package Code Package Description Billing Unit
166492-038-0259 mL in 1 BOTTLE, GLASS (66492-038-02)

NDC Record

Field Name Field Value Definition
PRODUCT NDC66492-038The 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 NAMELung DropsThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBelladonna, Ipecacuanha, Lobelia Inflata, Quebracho, Antimonium Tartaricum, Blatta Orientalis, Naphthalinum, Natrum Sulphuricum, Pulsatilla, Rumex Crispus, Mercurius Solubilis, Adrenalinum.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 NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/25/2014This 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 NAMEBe Well Medical dba Richard Clement Nutrition y Be Well HomeopathicsName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANEMONE PULSATILLA; ANTIMONY POTASSIUM TARTRATE; ASPIDOSPERMA QUEBRACHO-BLANCO BARK; ATROPA BELLADONNA; BLATTA ORIENTALIS; EPINEPHRINE; IPECAC; LOBELIA INFLATA; MERCURIUS SOLUBILIS; NAPHTHALENE; RUMEX CRISPUS ROOT; SODIUM SULFATEAn 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 STRENGTH6; 6; 5; 4; 6; 5; 4; 4; 8; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_C]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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