NDC 57520-0480 Envirostat

Berberis Vulgaris, Chelidonium Majus, Lappa Major, Phytolacca Decandra, Calcarea Fluorica, Carbo Animalis, Nux Vomica,

NDC Product Code 57520-0480

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: Berberis Vulgaris, Chelidonium Majus, Lappa Major, Phytolacca Decandra, Calcarea Fluorica, Carbo Animalis, Nux Vomica, 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.


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 a human over the counter drug product labeled by Apotheca Company. The generic name of Envirostat is berberis vulgaris, chelidonium majus, lappa major, phytolacca decandra, calcarea fluorica, carbo animalis, nux vomica,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Apotheca Company

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.


Envirostat 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.

  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • CALCIUM FLUORIDE 12 [hp_X]/mL
  • CARBO ANIMALIS 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • SULFUR 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL

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)

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.

* 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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