Vaccines

Arnica Montana, Hypericum Perforatum, Ledum Palustre, Morbillinum, Natrum Muriaticum, Silicea, Sulphur Iodatum, Thuja Occidentalis, Urtica Urens

Liddell Laboratories, Inc.
Human Otc Drug
NDC 50845-0262

Vaccines also known as Arnica Montana, Hypericum Perforatum, Ledum Palustre, Morbillinum, Natrum Muriaticum, Silicea, Sulphur Iodatum, Thuja Occidentalis, Urtica Urens is a human otc drug labeled by 'Liddell Laboratories, Inc.'. National Drug Code (NDC) number for Vaccines is 50845-0262. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Vaccines drug includes Arnica Montana Whole - 3 [hp_X]/mL Hypericum Perforatum Whole - 6 [hp_X]/mL Measles Virus - 30 [hp_X]/mL Rhododendron Tomentosum Leafy Twig - 30 [hp_C]/mL Silicon Dioxide - 30 [hp_C]/mL Sodium Chloride - 6 [hp_X]/mL Sulfur Iodide - 300 [hp_C]/mL Thuja Occidentalis Leafy Twig - 200 [hp_C]/mL Urtica Urens Whole - 3 [hp_X]/mL . The currest status of Vaccines drug is Active.

Drug Information:

Drug NDC:	50845-0262
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Vaccines
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Arnica Montana, Hypericum Perforatum, Ledum Palustre, Morbillinum, Natrum Muriaticum, Silicea, Sulphur Iodatum, Thuja Occidentalis, Urtica Urens
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Liddell Laboratories, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ARNICA MONTANA WHOLE - 3 [hp_X]/mL HYPERICUM PERFORATUM WHOLE - 6 [hp_X]/mL MEASLES VIRUS - 30 [hp_X]/mL RHODODENDRON TOMENTOSUM LEAFY TWIG - 30 [hp_C]/mL SILICON DIOXIDE - 30 [hp_C]/mL SODIUM CHLORIDE - 6 [hp_X]/mL SULFUR IODIDE - 300 [hp_C]/mL THUJA OCCIDENTALIS LEAFY TWIG - 200 [hp_C]/mL URTICA URENS WHOLE - 3 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	06 Aug, 2020
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	23 Dec, 2025
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Liddell Laboratories, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UNII:	O80TY208ZW XK4IUX8MNB HT3R7C012Q 877L01IZ0P ETJ7Z6XBU4 451W47IQ8X L6L8KA2AA0 1NT28V9397 IHN2NQ5OF9
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
50845-0262-2	30 mL in 1 BOTTLE, DROPPER (50845-0262-2)	06 Aug, 2020	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Vaccines

Arnica Montana & more..

Liquid
Liddell Laboratories, Inc.
NDC: 50845-0262

Purpose:

Uses: may temporarily relieve the ill effects - not the therapeutic effects - of oral or injected vaccines. children and adults may expect temporary relief from symptoms such as: â¢ minor fever â¢ pain â¢ redness â¢ weakness â¢ lack of energy â¢ swelling** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

Vaccines arnica montana, hypericum perforatum, ledum palustre, morbillinum, natrum muriaticum, silicea, sulphur iodatum, thuja occidentalis, urtica urens arnica montana whole arnica montana hypericum perforatum whole hypericum perforatum rhododendron tomentosum leafy twig ledum palustre twig measles virus measles virus sodium chloride chloride ion silicon dioxide silicon dioxide sulfur iodide sulfur iodide thuja occidentalis leafy twig thuja occidentalis leafy twig urtica urens whole urtica urens water alcohol

Indications and Usage:

Indications: may temporarily relieve the ill effects - not the therapeutic effects - of oral or injected vaccines. children and adults may expect temporary relief from symptoms such as: â¢ minor fever â¢ pain â¢ redness â¢ weakness â¢ lack of energy â¢ swelling** **claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: do not use if you have ever had an allergic reaction to this product or any of its ingredients. ask a doctor before use if excessive redness or swelling is present. stop use and ask a doctor if symptoms persist for more than 7 days, worsen, or if new symptoms occur. keep out of reach of children. in case of overdose, get medical help or call a poison control center right away. if pregnant or breast feeding, ask a doctor before using product. do not use if tamper evident seal around neck of bottle is missing or broken. other information: store at room temperature.

Dosage and Administration:

Directions: adults & children over 12: place 15 drops under the tongue 3 times per day. children 2 to 12: administer 1 drop under the tongue per year of age, 3 times per day. children 1 and under: administer 1 drop under the tongue, 3 times per day. for recent vaccinations, use daily for two weeks. for old vaccinations, use daily for one month. consult a physician for use in children under 12.

Package Label Principal Display Panel:

Package label display: oral drops liddell laboratories est. 1994 detox 50 vac vaccines may relieve the ill effects of vaccines: minor fever, pain, swelling, fatigue. homeopathic doctor formulated readily absorbed. safe. no known side effects. easy to use. 1.0 fl. oz. (30 ml) vaccines lbl vaccines ctn

Further Questions:

Questions: dist. by liddell laboratories inc. 201 apple blvd. woodbine, ia 51579 www.liddell.net 1-800-460-7733

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.