1. Home
  2. Labeler Index
  3. Bocks Inc
  4. NDC Product Code: 81527-001 Foaming Hand Sanitizer Refill Moisturizing Aloe

NDC 81527-001 Foaming Hand Sanitizer Refill Moisturizing Aloe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81527-001?
  4. Foaming Hand Sanitizer Refill Moisturizing Aloe 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:
81527-001
Proprietary Name:
Foaming Hand Sanitizer Refill Moisturizing Aloe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bocks Inc
Labeler Code:
81527
Product Label ID:
18e15a27-b6ce-4bfa-933c-405e8011639d
Start Marketing Date: [9]
02-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 81527-001?

The NDC code 81527-001 is assigned by the FDA to the product Foaming Hand Sanitizer Refill Moisturizing Aloe which is product labeled by Bocks Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 81527-001-16 473 ml in 1 carton , 81527-001-32 946 ml in 1 carton . 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 Foaming Hand Sanitizer Refill Moisturizing Aloe?

• pour liquid into a foaming dispenser • pump a small amount of foam into palm of hand • spread thoroughly on both hands • rub hands together until dry

Which are Foaming Hand Sanitizer Refill Moisturizing Aloe UNII Codes?

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

Which are Foaming Hand Sanitizer Refill Moisturizing Aloe 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 Foaming Hand Sanitizer Refill Moisturizing Aloe?

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:

* 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".