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  4. NDC Product Code: 73893-002 Hydra Pearl Hand Sanitizer

NDC 73893-002 Hydra Pearl Hand Sanitizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73893-002?
  4. Hydra Pearl Hand Sanitizer Uses
  5. 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:
73893-002
Proprietary Name:
Hydra Pearl Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Plasmadent Inc
Labeler Code:
73893
Product Label ID:
a0fbf042-4f3d-53c3-e053-2a95a90a877b
Start Marketing Date: [9]
08-12-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 73893-002?

The NDC code 73893-002 is assigned by the FDA to the product Hydra Pearl Hand Sanitizer which is product labeled by Plasmadent Inc. The product's dosage form is . The product is distributed in 8 packages with assigned NDC codes 73893-002-02 236.6 ml in 1 bottle, dispensing , 73893-002-03 473.2 ml in 1 bottle, dispensing , 73893-002-04 295.7 ml in 1 bottle, dispensing , 73893-002-05 946.4 ml in 1 bottle, dispensing , 73893-002-06 3800 ml in 1 container , 73893-002-08 18900 ml in 1 container , 73893-002-11 59.1 ml in 1 tube , 73893-002-12 189000 ml in 1 drum . 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 Hydra Pearl Hand Sanitizer?

Directions-wet hands thoroughly with product and allow to dry without wiping. For children under 6 use only under adult supervision. Not recommended for infants.

What is the NDC to RxNorm Crosswalk for Hydra Pearl Hand Sanitizer?

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:

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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".