NDC 68428-864 Aconitum Lycoctonum
Pellet Oral

Product Information

Aconitum Lycoctonum is a human over the counter drug product labeled by Washington Homeopathic Products. The product's dosage form is pellet and is administered via oral form.

Product Code68428-864
Proprietary Name 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.
Aconitum Lycoctonum
Non-Proprietary Name 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.
Aconitum Lycoctonum
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.
Human Otc Drug
Dosage FormPellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
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.
Washington Homeopathic Products
Labeler Code68428
Marketing Category 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.
UNAPPROVED HOMEOPATHIC -
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
10-11-2011
Listing Expiration Date 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.
12-31-2022
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Aconitum Lycoctonum?


Product Characteristics

Color(s)WHITE (C48325 - WHITE)

Product Packages

NDC 68428-864-03

Package Description: 75 PELLET in 1 VIAL, GLASS

NDC 68428-864-05

Package Description: 150 PELLET in 1 VIAL, GLASS

NDC 68428-864-06

Package Description: 1200 PELLET in 1 BOTTLE, GLASS

NDC 68428-864-11

Package Description: 300 PELLET in 1 BOTTLE, GLASS

NDC 68428-864-12

Package Description: 600 PELLET in 1 BOTTLE, GLASS

Product Details

What are Aconitum Lycoctonum Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

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.
  • SUCROSE (UNII: C151H8M554)
  • LACTOSE (UNII: J2B2A4N98G)

* Please review the disclaimer below.

Aconitum Lycoctonum Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredients



ACONITUM LYC 30C


Uses



To relieve the symptoms of fainting.


Keep Out Of Reach Of Children



Keep this and all medicines out of reach of children.


Indications



Indications:

ACONITUM LYC Lightheadedness


Stop Use And Ask Doctor



If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.


Directions



Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.


Inactive Ingredients



Sucrose/Lactose


Principal Display Panel



The OTC potency range of ACONITUM LYC is 3x–30x, 2c–30c, 200c, 1m, 10m, 50m, and CM.
Availability is subject to change.

All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.


* Please review the disclaimer below.