NDC 62795-1126 Hendel Psoriasis, Eczema, Seborrhea

Kerosene, Graphite, Calcium Sulfide, Sepia Officinalis Juice, Sulfur, And Thuja Occidentalis Leafy Twig

NDC Product Code 62795-1126

NDC CODE: 62795-1126

Proprietary Name: Hendel Psoriasis, Eczema, Seborrhea 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: Kerosene, Graphite, Calcium Sulfide, Sepia Officinalis Juice, Sulfur, 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
    • 62795-1126 - Hendel Psoriasis, Eczema, Seborrhea

NDC 62795-1126-2

Package Description: 100 TABLET in 1 BOTTLE

NDC Product Information

Hendel Psoriasis, Eczema, Seborrhea with NDC 62795-1126 is a a human over the counter drug product labeled by Medinatura Inc. The generic name of Hendel Psoriasis, Eczema, Seborrhea is kerosene, graphite, calcium sulfide, sepia officinalis juice, sulfur, 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.

Hendel Psoriasis, Eczema, Seborrhea 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.

  • KEROSENE 6 [hp_X]/1
  • GRAPHITE 12 [hp_X]/1
  • CALCIUM SULFIDE 12 [hp_X]/1
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/1
  • SULFUR 12 [hp_X]/1
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [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 MONOHYDRATE (UNII: EWQ57Q8I5X)
  • 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: 07-07-2016 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: 12-31-2021 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.

Hendel Psoriasis, Eczema, Seborrhea Product Label Images

Hendel Psoriasis, Eczema, Seborrhea 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

Warnings

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Psoriasis, Eczema, Seborrhea Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

Uses

• Red scaly patches on skin• Itchy• Flaky skin• Skin inflammation

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Directions

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

Indications

Psoriasis, Eczema, Seborrhea Relief

Inactive Ingredient

Lactose, Magnesium stearate

Ingredients

Each tablet contains equal parts of Petroleum 6X; Graphites 12X; Hepar sulphuris calcareum 12X; Sepia 12X; Sulphur 12X; Thuja occidentalis 12X.

* Please review the disclaimer below.