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  4. NDC Product Code: 79071-1004 Hand Sanitizer 8oz

NDC 79071-1004 Hand Sanitizer 8oz

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79071-1004?
  4. Hand Sanitizer 8oz 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:
79071-1004
Proprietary Name:
Hand Sanitizer 8oz
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Riviera Beverages, Llc
Labeler Code:
79071
Product Label ID:
ade298dd-1334-6c7e-e053-2a95a90ada40
Start Marketing Date: [9]
02-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79071-1004-0

Package Description: 250 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 79071-1004?

The NDC code 79071-1004 is assigned by the FDA to the product Hand Sanitizer 8oz which is product labeled by Riviera Beverages, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79071-1004-0 250 ml in 1 bottle, plastic . 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 Hand Sanitizer 8oz?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

What is the NDC to RxNorm Crosswalk for Hand Sanitizer 8oz?

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".