NDC 52731-7048 Leg Cramp Complex

NDC Product Code 52731-7048

NDC 52731-7048-2

Package Description: 1 BOTTLE in 1 BOX > 50 mL in 1 BOTTLE (52731-7048-1)

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

NDC Product Information

Leg Cramp Complex with NDC 52731-7048 is a product labeled by Nova Homeopathic Therapeutics, Inc.. The generic name of Leg Cramp Complex is . The product's dosage form is and is administered via form.

Labeler Name: Nova Homeopathic Therapeutics, Inc.

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)

Product Labeler Information

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

Labeler Name: Nova Homeopathic Therapeutics, Inc.
Labeler Code: 52731
Start Marketing Date: 06-01-2011 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 - INACTIVATED, the listing data was inactivated by the FDA. 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.

Leg Cramp Complex 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

Purpose:

Suggested use for one or more of the following symptoms:Cramps or stiffness in legs or feet, nighttime cramps in calves, cramps while walking.

Usage And Dosage:

For oral use only.

Dosage & Administration

Adults:    In Acute Phase:            20 drops, every half hour until relief occurs    When Relief Occurs:            12-15 drops, 4-6 times per dayChildren 6-12 years:            10 drops, 4-6 times per day

Warnings:

Keep out of reach of children.

Warnings

If symptoms persist, consult a physician.Do not use if ring on bottom of cap is broken or missing.

Active Ingredients:

Calcarea carbonica 8x, Colocynthis 4x, Cuprum aceticum 4x, Lacticum acidum 6x, Rhus toxicodendron 6x, Secale cornutum 6x, Veratrum album 6x

Inactive Ingredients:

Alcohol, 20% USP

Otc - Questions

Manufactured by Nova Homeopathic Therapeutics Inc., Albuquerque, New Mexico USA 871091-800-225-8094

* Please review the disclaimer below.