NDC 44911-0485 Bactestat

Baptisia Tinctoria, Echinacea (angustifolia), Phytolacca Decandra, Aconitum Napellus, Arsenicum Album, Belladonna, Ferrum Phosphoricum, Lachesis Mutus, Phosphorus

NDC Product Code 44911-0485

NDC Code: 44911-0485

Proprietary Name: Bactestat Additional informationCallout TooltipWhat 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: Baptisia Tinctoria, Echinacea (angustifolia), Phytolacca Decandra, Aconitum Napellus, Arsenicum Album, Belladonna, Ferrum Phosphoricum, Lachesis Mutus, Phosphorus Additional informationCallout TooltipWhat 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
  • 44911 - Energique, Inc.
    • 44911-0485 - Bactestat

NDC 44911-0485-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Bactestat with NDC 44911-0485 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Bactestat is baptisia tinctoria, echinacea (angustifolia), phytolacca decandra, aconitum napellus, arsenicum album, belladonna, ferrum phosphoricum, lachesis mutus, phosphorus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, Inc.

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 Additional informationCallout TooltipWhat 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.


Bactestat Active Ingredient(s)

Additional informationCallout TooltipWhat is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 6 [hp_X]/mL
  • ACONITUM NAPELLUS 12 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • ATROPA BELLADONNA 12 [hp_X]/mL
  • FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
  • LACHESIS MUTA VENOM 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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)

Additional informationCallout TooltipWhat 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

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Bactestat Product Label Images

Bactestat 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

Active Ingredients:

(in each drop): 14.26% of Aconitum Napellus 12X, Arsenicum Album 12X, Belladonna 12X, Ferrum Phosphoricum 12X, Lachesis Mutus 12X, Phosphorus 12X, Phytolacca Decandra 6X; 0.10% of Baptisia Tinctoria 3X, Echinacea (Angustifolia) 3X.

Indications:

May temporarily relieve fever, irritated throat, and acute irritation of the bladder.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve fever, irritated throat, and acute irritation of the bladder.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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.Warning: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult physician promptly. Do not use more than 2 days or administer to children under 3 years of age unless directed by a physician.

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.

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 Ingredients:

Demineralized water, 20% Ethanol.

Questions:

Dist. by Energique, Inc.201 Apple Blvd.Woodbine, IA 51579  800.869.8078

Package Label Display:

ENERGIQUESINCE 1987HOMEOPATHIC REMEDYBACTESTAT2 fl. oz. (60 ml)

* Please review the disclaimer below.

Previous Code
44911-0484
Next Code
44911-0486