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  4. NDC Product Code: 73694-101 Keep Going Sting Relief Pad

NDC 73694-101 Keep Going Sting Relief Pad

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73694-101?
  4. Keep Going Sting Relief Pad Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73694-101
Proprietary Name:
Keep Going Sting Relief Pad
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hk Top Sun Enterprise Co., Limited
Labeler Code:
73694
Product Label ID:
b4b22554-b35e-4f9d-a8d0-d7293e50725a
Start Marketing Date: [9]
03-14-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73694-101-01

Package Description: .4 g in 1 PACKAGE

Product Details

What is NDC 73694-101?

The NDC code 73694-101 is assigned by the FDA to the product Keep Going Sting Relief Pad which is product labeled by Hk Top Sun Enterprise Co., Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73694-101-01 .4 g in 1 package . 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 Keep Going Sting Relief Pad?

Adults and children 2 years of age or older . Cnsult physician for chldren under 2 years old. Do not apply more than 3 or 4 times daily. Wipe affected area to alleviate pain and itching. Discard after use.

Which are Keep Going Sting Relief Pad UNII Codes?

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

Which are Keep Going Sting Relief Pad 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:

What is the NDC to RxNorm Crosswalk for Keep Going Sting Relief Pad?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 895749 - benzocaine 6 % / isopropyl alcohol 60 % Medicated Pad
  • RxCUI: 895749 - benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated Pad
  • RxCUI: 895749 - benzocaine 6 % / isopropyl alcohol 60 % Topical Swab

* Please review the disclaimer below.

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".