NDC 51393-7222 Shingles Control

  1. Labeler Index
  2. Forces Of Nature
  3. NDC: 51393-7222 Shingles Control

NDC Product Code 51393-7222

NDC CODE: 51393-7222

Proprietary Name: Shingles Control What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 51393-7222-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC 51393-7222-2

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 51393-7222 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.

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: 09-01-2010 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: 12-31-2017 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 Label Images

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

Indications

For the temporary relief of inflammation, itching and redness associated with shingles.

Otc - Purpose

Homeopathic Active IngredientsThe letters 'HPUS' indicate that the components in this product are officially monographed in the Homœopathic Pharmacopœia of the United States.Equal parts of:PurposeCalendula Officinalis 6X HPUS Promotes healthy skin Geranium Maculatuum 6X HPUSHealing for ulcers in skinNatrum Muriaticum 6X HPUS Remedy for herpes, skin eruptions, hives Ranunculus Bulbosus 6X HPUS Remedy for herpes, shingles, burning, itching

Inactive Ingredients

Eucalypus Radiata Oil, Lavandin Oil, Palmarosa Oil, Tea Tree

Directions

Apply to area of outbreak. For best results apply immediately at the first sign of an outbreak. Apply 3-5 times per day during an outbreak or when you feel one coming on. Use of this product during the prodrome phase (tingling before the outbreak that some people experience) improves results. It may also be helpful to rub this oil on the soles of your feet 3 times per day during an outbreak.

Otc - When Using

If symptoms of pain and swelling worsen consult a health care professional. 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.

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. If accidental ingestion, get medical help or contact a Poison Control Center. For external use only. Do not apply to the eyes or mucous membranes. Keep all medicines out of the reach of children.

Otc - Stop Use

Stop use and ask a doctor if condition worsens or symptoms last more than 7 days.

Product Questions?

877-975-3797

* Please review the disclaimer below.