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  4. NDC Product Code: 72691-0929 Tick-me-off

NDC 72691-0929 Tick-me-off

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72691-0929?
  4. Tick-me-off Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72691-0929
Proprietary Name:
Tick-me-off
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pillar Health Systems Llc
Labeler Code:
72691
Product Label ID:
8d349800-232a-0c71-e053-2a95a90a41d0
Start Marketing Date: [9]
07-08-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72691-0929-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 72691-0929?

The NDC code 72691-0929 is assigned by the FDA to the product Tick-me-off which is product labeled by Pillar Health Systems Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72691-0929-1 30 ml in 1 bottle, dropper . 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 Tick-me-off?

For the temporary repellent of insects, such as but not limited to ticks, and the relief of symptoms due to insect bites such as skin irritation, redness, swelling, and itching.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary repellent of insects, such as but not limited to ticks, and the relief of symptoms due to insect bites such as skin irritation, redness, swelling, and itching.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Which are Tick-me-off UNII Codes?

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

Which are Tick-me-off 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:

* 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".