NDC 51393-7222 Shingles Control

Table of Contents

    1. Product Information
    2. Product Packages
    3. Product Characteristics
    4. What is NDC 51393-7222?
    5. Shingles Control Uses
    6. Active Ingredients UNII Codes

Product Information

NDC Product Code51393-7222
Proprietary Name 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.		Shingles Control
NDC Directory StatusINACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Forces Of Nature
Labeler Code51393
SPL SET ID:04d75d66-8c69-4bf3-9872-ca37d86b244a
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		09-01-2010
Listing Expiration Date 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.		12-31-2017
Exclude Flag 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". 		I
NDC Code Structure

Product Characteristics

Color(s)YELLOW (C48330)

Product Packages

NDC Code 51393-7222-1

Package Description: 11 mL in 1 BOTTLE, DISPENSING

NDC Code 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.

Product Details

What is NDC 51393-7222?

The NDC code 51393-7222 is assigned by the FDA to the product Shingles Control which is product labeled by Forces Of Nature. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 51393-7222-1 11 ml in 1 bottle, dispensing , 51393-7222-2 33 ml in 1 bottle, dispensing . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Shingles Control?

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

Which are Shingles Control UNII Codes?

The UNII codes for the active ingredients in this product are:

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
  • GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ)
  • GERANIUM MACULATUM ROOT (UNII: 93IXI5B6OJ) (Active Moiety)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
  • RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB)
  • RANUNCULUS BULBOSUS (UNII: AEQ8NXJ0MB) (Active Moiety)

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