NDC 42681-0508 Arnica Montana

NDC Product Code 42681-0508

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Arnica Montana with NDC 42681-0508 is a product labeled by Whole Foods Market. The generic name of Arnica Montana is . The product's dosage form is and is administered via form.

Labeler Name: Whole Foods Market

Dosage Form: -

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.

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.

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

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Whole Foods Market
Labeler Code: 42681
Start Marketing Date: 11-23-2011 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: 12-31-2017 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: I 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.

Arnica Montana 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 Ingredient: Arnica Montana HPUS 30c

Dosage & Administration

Directions: (adults and children 12 years and older) Dissolve 5 pellets under the tongue 3
times per day until symptoms are relieved or as directed by a doctor.

Uses

For the conditions listed under purposes or as directed by a doctor.

Warnings

Warnings: Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding, ask a health care professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Other Safety Information

Store at room temperature.

Otc - Do Not Use

Other information: Do not use if pellet dispenser seal is broken.

Inactive Ingredient

Inactive Ingredients: Lactose, sucrose.

Otc - Purpose

Purposes: relief of muscle aches and soreness, swelling, stiffness and bruising.

* Please review the disclaimer below.