NDC 51393-6668 Nevi (mole) Control Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51393-6668
Proprietary Name:
Nevi (mole) Control Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
51393
Start Marketing Date: [9]
04-06-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Code Structure Chart

Product Details

What is NDC 51393-6668?

The NDC code 51393-6668 is assigned by the FDA to the product Nevi (mole) Control Extra Strength 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 51393-6668-1 11 ml in 1 bottle, dispensing , 51393-6668-2 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 Nevi (mole) Control Extra Strength?

Apply three times a day directly to mole(s) using a cotton swab, or apply directly with fingers and wash hands with warm soap and water. Avoid contact with the eyes. External use only.

Which are Nevi (mole) Control Extra Strength 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)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)

Which are Nevi (mole) Control Extra Strength Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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] 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".