NDC 62795-1011 Bhi Allergy

Antimony Trisulfide, Arnica Montana Root, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, Thuja Occidentalis Leafy Twig

NDC Product Code 62795-1011

NDC Code: 62795-1011

Proprietary Name: Bhi Allergy 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, Formic Acid, Graphite, Histamine Dihydrochloride,strychnos Ignatii Seed, Arctium Lappa Root, Ledum Palustre Twig, Lycopodium Clavatum Spore, Pine Tar, Selenium, Sulfur, Sulfuric Acid, Tellurium, 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
    • 62795-1011 - Bhi Allergy

NDC 62795-1011-2

Package Description: 100 TABLET in 1 BOTTLE

NDC Product Information

Bhi Allergy with NDC 62795-1011 is a a human over the counter drug product labeled by Medinatura. The generic name of Bhi Allergy is antimony trisulfide, arnica montana root, formic acid, graphite, histamine dihydrochloride,strychnos ignatii seed, arctium lappa root, ledum palustre twig, lycopodium clavatum spore, pine tar, selenium, sulfur, sulfuric acid, tellurium, thuja occidentalis leafy twig. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Medinatura

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.

Bhi Allergy 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.

  • FORMIC ACID 8 [hp_X]/1
  • GRAPHITE 10 [hp_X]/1
  • PINE TAR 10 [hp_X]/1
  • SELENIUM 12 [hp_X]/1
  • SULFUR 12 [hp_X]/1
  • SULFURIC ACID 30 [hp_X]/1
  • TELLURIUM 10 [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.


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
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: 08-30-2014 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: 12-31-2020 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.

Bhi Allergy Product Label Images

Bhi Allergy 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

Indication And Usage

For the temporary relief of minor allergy symptoms: runny nose, watery eyes, skin irritations


If pregnant or breast-feeding, ask a health professional before use. If symptoms persist or worsen, a healthcare professional should be consulted. Do not use if known sensitivity to BHI Allergy or any of its ingredients exists.

Dosage And Administration

At first sign of symptoms: Adults and children 4 years and older:1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. Do not exceed 12 tablets in 24 hoursStandard dosage: Adults and children 4 years and older:3 tablets per day, taking 1 tablet every 4 to 6 hours. For children under 4, consult you 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 6X, Formicumacidum 8X, Graphites 10X, Histaminum hydrochloricum 8X, 12X, 30X, 200X, *Ignatia amara 6X, *Lappa major 8X, *Ledum palustre 8X, *Lycopodium clavatum 6X, *Pix liquida 10X, Selenium metallicum 12X, *Sulphur 12X, Sulphuricum acidum 30X, *Tellurium metallicum 10X, *Thuja occidentalis 6X 16.7 mg each.*Natural ingredients

Inactive Ingredients

Inactive Ingredients: Lactose, Magnesium stearate


Relieves:• Runny Nose• Watery Eyes due to Hayfever• Mild Skin Rashes & Hives

* Please review the disclaimer below.

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