59623-004 NDC - BREATHE EASIER FORMULA (CUPRESSUS AUS, EUCALYPTUS, MENTHA PIP, ORIGANUM, PINUS SYL, SALVIA, KALI IOD, EUPHORBIUM, GALPHIMIA, HYDRASTIS, LUFFA, PULSATILLA, HEPAR SUPLH CALC, HISTAMINUM, KALI BIC.)

Drug Information

Product NDC: 59623-004

Proprietary Name: Breathe Easier Formula

Non Proprietary Name: Cupressus Aus, Eucalyptus, Mentha Pip, Origanum, Pinus Syl, Salvia, Kali Iod, Euphorbium, Galphimia, Hydrastis, Luffa, Pulsatilla, Hepar Suplh Calc, Histaminum, Kali Bic.

Active Ingredient(s):
  • 12 [hp_X]/mL CALCIUM SULFIDE;
  • 3 [hp_X]/mL CUPRESSUS SEMPERVIRENS FRUITING LEAFY TWIG;
  • 3 [hp_X]/mL EUCALYPTUS GLOBULUS LEAF;
  • 6 [hp_X]/mL EUPHORBIA RESINIFERA RESIN;
  • 6 [hp_X]/mL GALPHIMIA GLAUCA FLOWERING TOP;
  • 6 [hp_X]/mL GOLDENSEAL;
  • 12 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE;
  • 6 [hp_X]/mL LUFFA OPERCULATA FRUIT;
  • 3 [hp_X]/mL MENTHA PIPERITA;
  • 3 [hp_X]/mL ORIGANUM MAJORANA WHOLE;
  • 3 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG;
  • 12 [hp_X]/mL POTASSIUM DICHROMATE;
  • 4 [hp_X]/mL POTASSIUM IODIDE;
  • 6 [hp_X]/mL PULSATILLA VULGARIS;
  • 3 [hp_X]/mL SAGE


Administration Route(s): NASAL

Dosage Form(s): SPRAY

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

Labeler Information

Labeler Name: Integrative Healing Institute, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/23/2013

Package Information

No. Package Code Package Description Billing Unit
159623-004-0330 mL in 1 BOTTLE, SPRAY (59623-004-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59623-004The 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 NAMEBreathe Easier FormulaThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECupressus Aus, Eucalyptus, Mentha Pip, Origanum, Pinus Syl, Salvia, Kali Iod, Euphorbium, Galphimia, Hydrastis, Luffa, Pulsatilla, Hepar Suplh Calc, Histaminum, Kali Bic.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMENASALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE9/23/2013This 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 NAMEIntegrative Healing Institute, LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCIUM SULFIDE; CUPRESSUS SEMPERVIRENS FRUITING LEAFY TWIG; EUCALYPTUS GLOBULUS LEAF; EUPHORBIA RESINIFERA RESIN; GALPHIMIA GLAUCA FLOWERING TOP; GOLDENSEAL; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; MENTHA PIPERITA; ORIGANUM MAJORANA WHOLE; PINUS SYLVESTRIS LEAFY TWIG; POTASSIUM DICHROMATE; POTASSIUM IODIDE; PULSATILLA VULGARIS; SAGEAn 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 STRENGTH12; 3; 3; 6; 6; 6; 12; 6; 3; 3; 3; 12; 4; 6; 3 
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 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] 

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