NDC 62795-1028 Clearlife

Antimony Trisulfide, Arnica Montana Root, Euphrasia Stricta,formic Acid,graphite,histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, And Thuja Occidentalis Leafy Twig

NDC Product Code 62795-1028

NDC Code: 62795-1028

Proprietary Name: Clearlife What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Antimony Trisulfide, Arnica Montana Root, Euphrasia Stricta,formic Acid,graphite,histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, And Thuja Occidentalis Leafy Twig What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 62795 - Medinatura Inc.
    • 62795-1028 - Clearlife

NDC 62795-1028-2

Package Description: 1 BOTTLE in 1 CARTON > 100 TABLET in 1 BOTTLE

NDC Product Information

Clearlife with NDC 62795-1028 is a a human over the counter drug product labeled by Medinatura Inc.. The generic name of Clearlife is antimony trisulfide, arnica montana root, euphrasia stricta,formic acid,graphite,histamine dihydrochloride,strychnos ignatii seed, arctium lappa root, ledum palustre twig, lycopodium clavatum spore, pine tar, selenium, sulfur, sulfuric acid, tellurium, and thuja occidentalis leafy twig. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Medinatura Inc.

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Clearlife Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ANTIMONY TRISULFIDE 10 [hp_X]/1
  • ARNICA MONTANA ROOT 5 [hp_X]/1
  • EUPHRASIA STRICTA 6 [hp_X]/1
  • FORMIC ACID 8 [hp_X]/1
  • GRAPHITE 10 [hp_X]/1
  • HISTAMINE DIHYDROCHLORIDE 8 [hp_X]/1
  • STRYCHNOS IGNATII SEED 6 [hp_X]/1
  • ARCTIUM LAPPA ROOT 8 [hp_X]/1
  • LEDUM PALUSTRE TWIG 7 [hp_X]/1
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/1
  • PINE TAR 10 [hp_X]/1
  • SELENIUM 12 [hp_X]/1
  • SULFUR 12 [hp_X]/1
  • SULFURIC ACID 21 [hp_X]/1
  • TELLURIUM 10 [hp_X]/1
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • LACTOSE (UNII: J2B2A4N98G)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Medinatura Inc.
Labeler Code: 62795
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 09-30-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Clearlife Product Label Images

Clearlife Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Keep Out Of Reach Of Children

Keep out of reach of children.

Indications And Usage

  • For the temporary relief of minor allergy symptoms:Runny noseWatery eyesSkin irritations

Warnings

If pregnant or breast-feeding, ask a healthcare provider before use. Keep out of reach of children. If symptoms persist or worsen, a healthcare provider should be consulted. Do not use if known sensitivity to ClearLife™ or any of its ingredients exists.

Dosage And Administration

Standard Dosage:Adults and children 12 years and older: 3 tablets per day, taking 1 tablet every 4 to 6 hours.Children 4 to 11 years: 2 tablets per day, taking 1 tablet every 6 to 8 hours.Children under 4 years, consult your healthcare provider.Initial Dosage:Adults and children 12 years and older: 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceeed 12 tablets in 24 hours.Children 4 to 11 years: 1 tablet every 1/2 to 1 hour, until symptoms lessen, then continue with standard dosage. Do not exceed 8 tablets in 24 hours.Children under 4 years, consult your healthcare provider.Allow tablets to dissolve completely in the mouth, do not swallow.

Active Ingredients

Active Ingredients: Each tablet contains: Antimonium crudum 10X, *Arnica montana, radix 5X,*Euphrasia officinalis 6X, Formicum acidum 8X, Graphites 10X, Histaminum hydrochloricum 8X, Histaminum hydrochloricum 12X, Histaminum hydrochloricum 20X, *Ignatia amara 5X, *Lappa major 8X, *Ledum palustre 7X, *Lycopodium clavatum 6X, *Pix liquida 10X, Selenium metallicum 12X, *Sulphur 12X, Sulphuricum acidum 21X, *Tellurium metallicum 10X, *Thuja occidentalis 6X.*Natural Ingredients

Purpose

Antimonium crudum 10X..............................Relieves skin rashesArnica montana, radix 6X............................Relieves itching skinEuphrasia officinalis 6X..............................Relieves allergic eye symptomsFormicum acidum 8X...................................Relieves dry throatGraphites 10X.............................................Relieves skin irritationsHistaminum hydrochloricum 8X, 12X, 20X....Relieves allergic itchIgnatia amara 5X.......................................Relieves tickling in throatLappa major 8X..........................................Relieves itchy, Irritated skinLedum palustre 7X.....................................Relieves Itchy skinLycopodium clavatum 6X............................Relieves nasal congestionPix liquida 10X...........................................Relieves itchy skinSelenium metallicum 12X...........................Relieves skin rashesSulphur 12X...............................................Relieves sneezingSulphuricum acidum 21X............................Relieves itchy, watery eyesTellurium metallicum 10X...........................Relieves itchy eyesThuja occidentalis 6X.................................Relieves nasal irritations

* Please review the disclaimer below.

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