NDC 57520-0480 Envirostat

NDC Product Code 57520-0480

This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Code: 57520-0480

Proprietary Name: Envirostat 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: 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

  • 57520 - Apotheca Company
    • 57520-0480 - Envirostat

NDC 57520-0480-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Envirostat with NDC 57520-0480 is a product labeled by Apotheca Company. The generic name of Envirostat is . The product's dosage form is and is administered via form.

Labeler Name: Apotheca Company

Dosage Form: -

Product Type: 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.

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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

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

Labeler Name: Apotheca Company
Labeler Code: 57520
Start Marketing Date: 06-04-2010 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: 12-31-2018 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: E 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.

Envirostat Product Label Images

Envirostat 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

Otc - Active Ingredient

ACTIVE INGREDIENTS:  Berberis vulgaris 3X, Chelidonium majus 3X, Lappa major 3X, Phytolacca decandra 3X, Calcarea fluorica 12X, Carbo animalis 12X, Nux Vomica 12X, Phosphorus 12X, Sepia 12X, Sulphur 12X, Thuja occidentalis 12X.

Otc - Purpose

INDICATIONS:  For temporary relief of head congestion and general exhaustion as a consequence of exposure to smog, dust, or industrial agents.

Warnings

WARNINGS:  If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children.In case of overdose, get medical help or contact a Poison Control Center right away.  Do not use if tamper evident seal is broken or missing.  Store in a cool, dry place.

Dosage & Administration

SUGGESTED USE:  Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional.  If symptoms persist, consult your health care professional.  Consult a physician for use in children under 12 hears of age.

Inactive Ingredient

INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol

Otc - Questions

Dist. By:Energique, Inc.201 Apple Blvd.Woodbine, IA 51579800-869-8078

* Please review the disclaimer below.

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