NDC 43406-0004 Anxiety Ii Hp

Aconitum Napellus, Arsenic Trioxide, Atropa Belladonna, Oyster Shell Calcium Carbonate, Crude, Activated Charcoal, Human Breast Tumor Cell, Causticum, Gelsemium Sempervirens Root, Lachesis Muta Venom, Mercury, Sodium Chloride, Nitric Acid, Phosphorus, Toxicodendron Pubescens Leaf

NDC Product Code 43406-0004

NDC CODE: 43406-0004

Proprietary Name: Anxiety Ii Hp 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: Aconitum Napellus, Arsenic Trioxide, Atropa Belladonna, Oyster Shell Calcium Carbonate, Crude, Activated Charcoal, Human Breast Tumor Cell, Causticum, Gelsemium Sempervirens Root, Lachesis Muta Venom, Mercury, Sodium Chloride, Nitric Acid, Phosphorus, Toxicodendron Pubescens Leaf 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

  • 43406 - Natural Creations, Inc.

NDC 43406-0004-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Anxiety Ii Hp with NDC 43406-0004 is a a human over the counter drug product labeled by Natural Creations, Inc.. The generic name of Anxiety Ii Hp is aconitum napellus, arsenic trioxide, atropa belladonna, oyster shell calcium carbonate, crude, activated charcoal, human breast tumor cell, causticum, gelsemium sempervirens root, lachesis muta venom, mercury, sodium chloride, nitric acid, phosphorus, toxicodendron pubescens leaf. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Natural Creations, 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 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.

Anxiety Ii Hp 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.

  • ACONITUM NAPELLUS WHOLE 30 [hp_C]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • ATROPA BELLADONNA 30 [hp_C]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
  • ACTIVATED CHARCOAL 30 [hp_C]/mL
  • HUMAN BREAST TUMOR CELL 30 [hp_C]/mL
  • CAUSTICUM 30 [hp_C]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/mL
  • LACHESIS MUTA VENOM 30 [hp_C]/mL
  • MERCURY 30 [hp_C]/mL
  • NITRIC ACID 30 [hp_C]/mL
  • PHOSPHORUS 30 [hp_C]/mL
  • TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL
  • SODIUM CHLORIDE 30 [hp_C]/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.

Labeler Name: Natural Creations, Inc.
Labeler Code: 43406
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-29-2007 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: 12-31-2021 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: N - NO 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.

Anxiety Ii Hp Product Label Images

Anxiety Ii Hp 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: Aconite Napellus 30C, Arsenicum Album 30C, Belladonna 30C, Calcarea Carbonica 30C, Carbo Vegetabilis 30C, Carcinosin 30C, Causticum 30C, Gelsemium Sempervirens 30C, Lachesis Mtus 30C, Mercurius Vivus 30C, Natrum Muriaticum 390C, Nitricum Acidum 30C, Phosporus 3C, Rhus Toxicodendron 30C

Indications & Usage

USES: Temporarily relieves anxieties, worries, fears, and/or oversensitive feelings.

Warnings

WARNING:Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

Dosage & Administration

DIRECTIONS: Take 10 drops orally, 3 times daily or as directed by a health care professional.

Otc - Do Not Use

OTHER INFORMATION: Tamper Seal: "Sealed for your protection."Do not use if seal is broken or missing.

Inactive Ingredient

INACTIVE INGREDIENTS: Purified Water, USP Ethanol Alcohol 20%

Otc - Questions

QUESTIONS AND COMMENTS?MFG FOR: Natural Creations / Woodbine, IA / 51579 712.647.1600LOT:

Otc - Purpose

USES: Temporarily relieves anxieties, worries, fears and/or oversensitive feelings.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center.

* Please review the disclaimer below.