62795-1050 NDC - CLEARLIFE EXTRA STRENGTH (ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, APIS MELLIFERA, ARNICA MONTANA WHOLE, EUPHRASIA STRICTA, GRAPHITE,GALPHIMIA GLAUCA FLOWERING TOP,PULSATILLA VULGARIS WHOLE, HISTAMINE DIHYDROCHLORIDE, PINE TAR, SCHOENOCAULON OFFICINALE SEED, SULFUR, SULFURIC ACID,TELLURIUM AND THUJA OCCIDENTALIS LEAFY TWIG)

Drug Information

  • Product NDC: 62795-1050
  • Proprietary Name: Clearlife Extra Strength
  • Non Proprietary Name: ONION, AMBROSIA ARTEMISIIFOLIA WHOLE, APIS MELLIFERA, ARNICA MONTANA WHOLE, EUPHRASIA STRICTA, GRAPHITE,GALPHIMIA GLAUCA FLOWERING TOP,PULSATILLA VULGARIS WHOLE, HISTAMINE DIHYDROCHLORIDE, PINE TAR, SCHOENOCAULON OFFICINALE SEED, SULFUR, SULFURIC ACID,TELLURIUM and THUJA OCCIDENTALIS LEAFY TWIG
  • Active Ingredient(s): 3 [hp_X]/1 AMBROSIA ARTEMISIIFOLIA WHOLE; 4 [hp_X]/1 APIS MELLIFERA; 5 [hp_X]/1 ARNICA MONTANA; 3 [hp_X]/1 EUPHRASIA STRICTA; 3 [hp_X]/1 GALPHIMIA GLAUCA FLOWERING TOP; 10 [hp_X]/1 GRAPHITE; 8 [hp_X]/1 HISTAMINE DIHYDROCHLORIDE; 3 [hp_X]/1 ONION; 10 [hp_X]/1 PINE TAR; 4 [hp_X]/1 PULSATILLA VULGARIS WHOLE; 6 [hp_X]/1 SCHOENOCAULON OFFICINALE SEED; 4 [hp_X]/1 SULFUR; 20 [hp_X]/1 SULFURIC ACID; 10 [hp_X]/1 TELLURIUM; 6 [hp_X]/1 THUJA OCCIDENTALIS LEAFY TWIG
  • Administration Route(s): ORAL
  • Dosage Form(s): TABLET
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Bee Venoms [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Food Allergenic Extract [EPC]; Standardized Insect Venom Allergenic Extract [EPC]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: MediNatura Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/6/2021

Package Information

No. Package Code Package Description Billing Unit
162795-1050-21 BOTTLE in 1 CARTON (62795-1050-2) / 60 TABLET in 1 BOTTLEEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC62795-1050The 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 NAMEClearlife Extra StrengthThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEONION, AMBROSIA ARTEMISIIFOLIA WHOLE, APIS MELLIFERA, ARNICA MONTANA WHOLE, EUPHRASIA STRICTA, GRAPHITE,GALPHIMIA GLAUCA FLOWERING TOP,PULSATILLA VULGARIS WHOLE, HISTAMINE DIHYDROCHLORIDE, PINE TAR, SCHOENOCAULON OFFICINALE SEED, SULFUR, SULFURIC ACID,TELLURIUM and THUJA OCCIDENTALIS LEAFY TWIGThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe 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 DATE1/6/2021This 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 NAMEMediNatura Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAMBROSIA ARTEMISIIFOLIA WHOLE; APIS MELLIFERA; ARNICA MONTANA; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; ONION; PINE TAR; PULSATILLA VULGARIS WHOLE; SCHOENOCAULON OFFICINALE SEED; SULFUR; SULFURIC ACID; TELLURIUM; THUJA OCCIDENTALIS LEAFY TWIGAn 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 STRENGTH3; 4; 5; 3; 3; 10; 8; 3; 10; 4; 6; 4; 20; 10; 6 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 
PHARM CLASSESAllergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS] 

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This page was last updated on: 5/26/2025

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