1. Home
  2. Labeler Index
  3. Integrity12 Inc
  4. NDC Product Code: 81111-100 Slow Corporation

NDC 81111-100 Slow Corporation

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81111-100?
  4. Slow Corporation 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:
81111-100
Proprietary Name:
Slow Corporation
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Integrity12 Inc
Labeler Code:
81111
Product Label ID:
b4942b2c-5480-3302-e053-2995a90a9bb7
Start Marketing Date: [9]
11-20-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81111-100-01

Package Description: 250 g in 1 BOTTLE

Product Details

What is NDC 81111-100?

The NDC code 81111-100 is assigned by the FDA to the product Slow Corporation which is product labeled by Integrity12 Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81111-100-01 250 g in 1 bottle . 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 Slow Corporation?

Directions:Adult and children 2 years of age and older: brush teeth thoroughly preferably after each meal or at least twice a day, or as directed by a dentist or physicianChildren 2 to 6 years: use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)Children under 2 years: ask a dentist or physician.

Which are Slow Corporation UNII Codes?

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

Which are Slow Corporation 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".