NDC 71919-404 Lappa Major

Arctium Lappa Root

NDC Product Code 71919-404

NDC 71919-404-07

Package Description: 15 mL in 1 VIAL, GLASS

NDC 71919-404-08

Package Description: 30 mL in 1 VIAL, GLASS

NDC 71919-404-09

Package Description: 50 mL in 1 BOTTLE, GLASS

NDC 71919-404-10

Package Description: 100 mL in 1 BOTTLE, GLASS

NDC Product Information

Lappa Major with NDC 71919-404 is a a human over the counter drug product labeled by Washington Homeopathic Products. The generic name of Lappa Major is arctium lappa root. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Washington Homeopathic Products

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.

Lappa Major 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.

  • ARCTIUM LAPPA ROOT 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.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

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: Washington Homeopathic Products
Labeler Code: 71919
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: 02-03-2010 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: 12-31-2020 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 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.

Lappa Major Product Label Images

Lappa Major 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

LAPPA

Uses

To relieve the symptoms of skin eruptions.

Keep Out Of Reach Of Children

Keep this and all medicines out of reach of children.

Indications

Indications: LAPPA   Skin eruptions

Stop Use And Ask Doctor

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

Directions

Adults: 4 drops into a tsp. of water 3 times a day. Children: 1/2 dose. Repeat at greater intervals as condition subsides. Or as directed bya lic. practitioner.

Inactive Ingredients

Sucrose/Lactose

* Please review the disclaimer below.

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