NDC 57520-0870 Infectistat

NDC Product Code 57520-0870

NDC 57520-0870-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Infectistat with NDC 57520-0870 is a product labeled by Apotheca Company. The generic name of Infectistat is . The product's dosage form is and is administered via form.

Labeler Name: Apotheca Company

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: 09-26-2011 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Infectistat Product Label Images

Infectistat 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:  Baptisia Tinctoria 3X, Echinacea 3X, Hydrastis Canadensis 3X, Lobelia Inflata 3X, Lomatium Dissectum 3X, Phytolacca Decandra 3X, Symphtum Officinale 3X, Lung 6X, Aconitum Napellus 12X, Arsenicum Album 12X, Belladonna 12X, Bryonia 12X, Causticum 12X, Eupatorium Perfoliatum 12X, Ferrum Phosphoricum 12X, Gelsemium Sempervirens 12X, Hypericum Perforatum 12X, Kali Carbonicum 12X, Lachesis Mutus 12X, Natrum Sulphuricum 12X, Phosphorus 12X, Pulsatilla 12X, Rhus Toxicodendron 12X, Silicea 12X, Sulphur 12X, Pyrogenium 30X.

Otc - Purpose

INDICATIONS:  For temporary relief of fever, sore throat, and cough due to bacterial and viral conditions.

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 years of age.

Inactive Ingredient

INACTIVE INGREDIENTS:  Demineralized water, 20% Ethanol.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.  In case of overdose, get medical help or contact Poison Control Center right away.

Indications & Usage

INDICATIONS:  For temporary relief of fever, sore throat, and cough due to bacterial and viral conditions.

Otc - Questions

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

* Please review the disclaimer below.