NDC 51393-7323 Shingles Control Extra Strength

NDC Product Code 51393-7323

NDC 51393-7323-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC 51393-7323-2

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 Extra Strength with NDC 51393-7323 is a product labeled by Forces Of Nature. The generic name of Shingles Control Extra Strength is . The product's dosage form is and is administered via form.

Labeler Name: Forces Of Nature

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 - 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Shingles Control Extra Strength Product Label Images

Shingles Control Extra Strength 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 8X HPUSPromotes healthy skinNatrum Muriaticum 8X HPUS Remedy for herpes, skin eruptions, hives Hypericum Perforatum 8X HPUSFor herpes zoster/shingles

Also Includes

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


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 - Do Not Use

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.