NDC 72764-003 The Eraser

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:
72764-003
Proprietary Name:
The Eraser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Brandable
Labeler Code:
72764
Start Marketing Date: [9]
02-28-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)

Product Packages

NDC Code 72764-003-01

Package Description: 1 PACKET in 1 CARTON / 14 SUPPOSITORY in 1 PACKET

Product Details

What is NDC 72764-003?

The NDC code 72764-003 is assigned by the FDA to the product The Eraser which is product labeled by Brandable. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72764-003-01 1 packet in 1 carton / 14 suppository in 1 packet. 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 The Eraser?

Remove one suppository from the foil wrap and place in the applicator. Insert suppository into the vagina with the applicator. Remove applicator and cleanse thoroughly with soap and water. Use one suppository daily for seven days.

Which are The Eraser UNII Codes?

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

  • SODIUM BORATE (UNII: 91MBZ8H3QO)
  • BORATE ION (UNII: 44OAE30D22) (Active Moiety)
  • COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR)
  • COLLINSONIA CANADENSIS ROOT (UNII: O2630F3XDR) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)

Which are The Eraser 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".