NDC 57955-9651 Endtag

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:
57955-9651
Proprietary Name:
Endtag
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
57955
Start Marketing Date: [9]
06-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 57955-9651?

The NDC code 57955-9651 is assigned by the FDA to the product Endtag which is product labeled by King Bio Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57955-9651-0 1 bottle, with applicator in 1 carton / 15 ml in 1 bottle, with applicator. 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 Endtag?

Shake before usingAdults and children 6 years of age and older: apply 3 times daily to affected area. Children under 6 years of age: Consult a doctor. Skin tag will dry and flake away over a period of 3-6 weeks.Some individuals may be senstitive to essential oil. Skin test for tolerability.

Which are Endtag UNII Codes?

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

  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N)
  • THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (Active Moiety)
  • ALOE SUCCOTRINA WHOLE (UNII: M6U8N4MD5P)
  • ALOE SUCCOTRINA WHOLE (UNII: M6U8N4MD5P) (Active Moiety)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)

Which are Endtag 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".