NDC 54532-0035 Hevert Contrallergia

Apis Mellifera, Galphimia Glauca Whole, Potassium Dichromate, Teucrium Marum Top, And Verbascum Densiflorum Flowering Top

NDC Product Code 54532-0035

NDC CODE: 54532-0035

Proprietary Name: Hevert Contrallergia 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: Apis Mellifera, Galphimia Glauca Whole, Potassium Dichromate, Teucrium Marum Top, And Verbascum Densiflorum Flowering Top 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

  • 54532 - Hevert Pharmaceuticals Llc

NDC 54532-0035-4

Package Description: 10 BLISTER PACK in 1 CARTON > 10 TABLET in 1 BLISTER PACK

NDC Product Information

Hevert Contrallergia with NDC 54532-0035 is a a human over the counter drug product labeled by Hevert Pharmaceuticals Llc. The generic name of Hevert Contrallergia is apis mellifera, galphimia glauca whole, potassium dichromate, teucrium marum top, and verbascum densiflorum flowering top. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Hevert Pharmaceuticals Llc

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.

Hevert Contrallergia 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.

  • APIS MELLIFERA 4 [hp_X]/1

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: Hevert Pharmaceuticals Llc
Labeler Code: 54532
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: 12-01-2019 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’.

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Hevert Contrallergia Product Label Images