NDC 51393-7322 Shingles Control

NDC Product Code 51393-7322

NDC 51393-7322-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC 51393-7322-2

Package Description: 33 mL in 1 BOTTLE, DISPENSING

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

NDC Product Information

Shingles Control with NDC 51393-7322 is a product labeled by Forces Of Nature. The generic name of Shingles Control is . The product's dosage form is and is administered via form.

Labeler Name: Forces Of Nature

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.


Product Labeler Information

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

Labeler Name: Forces Of Nature
Labeler Code: 51393
Start Marketing Date: 04-06-2011 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.

Shingles Control 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


Drug Facts

Product Note: Shingles is a viral infection (herpes zoster) of the skin with symptoms of rashes or blisters, redness and pain. Viral infections are often highly contagious.

Otc - Purpose

Active IngredientsThe letters 'HPUS' indicate that the component(s) in this product is (are) officially monographed in the Homœopathic Pharmacopœia of the United States.Equal parts of:PurposeCalendula Officinalis 6X HPUSPromotes healthy skinNatrum Muriaticum 6X HPUS Remedy for herpes, skin eruptions, hivesHypericum Perforatum 6X HPUSFor herpes zoster/shingles

Also Includes

Certified Organic Oils of: Eucalypus Radiata Leaf, French Lavandin Super, Napalese Palmarosa, Tea Tree


Apply to affected area at first sign of an outbreak 3-5 times per day. Avoid contact with eyes.


For relief and treatment of skin inflammation, pain and redness of shingles outbreaks.

Otc - Ask Doctor

If skin symptoms worsen consult a health care professional.

Otc - Stop Use

Some individuals may be sensitive to tea tree or other oils. Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin.

Stop use and ask a doctor if condition worsens or symptoms last more than 7 days or clear up and occur again within a few days.

Otc - Pregnancy Or Breast Feeding

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

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

Keep all medicines out of the reach of children.

Otc - When Using

External use only. If accidental ingestion, get medical help or contact a Poison Control Center.Do not apply to the eyes or mucous membranes.

* Please review the disclaimer below.