NDC 44911-0015 Allerstat II

NDC Product Code 44911-0015

NDC 44911-0015-1

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

Allerstat II with NDC 44911-0015 is a product labeled by Energique, Inc.. The generic name of Allerstat II is . The product's dosage form is and is administered via form.

Labeler Name: Energique, Inc.

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: Energique, Inc.
Labeler Code: 44911
Start Marketing Date: 07-17-2012 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: 12-31-2019 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 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.

Allerstat II Product Label Images

Allerstat II 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, Allium cepa 12X, Ambrosia artemisiaefolia 12X, Arsenicum album 12X, Euphrasia officinalis 12X, Natrum sulphuricum 12X, Nux vomica 12X, Phosphorus 12X, Pulsatilla 12X, Solidago virgaurea 12X, Sulphur 12X.

Otc - Purpose

INDICATIONS:  For temporary relief of sinus congestion due to hay fever and allergic rhinitis. ****These statements are based upon traditional homeopathic
practice.  They have not been reviewed by the Food and Drug
Administration.

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

DIRECTIONS:  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 a Poison Control Center right
away.

Otc - Questions

​Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579800-869-8078

Indications & Usage

INDICATIONS:  For temporary relief of sinus congestion due to hay fever and allergic rhinitis. ****These statements are based upon traditional homeopathic
practice.  They have not been reviewed by the Food and Drug
Administration.

* Please review the disclaimer below.