NDC 78677-800 Purevita 80% Hand Sanitizer Gel

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
78677-800
Proprietary Name:
Purevita 80% Hand Sanitizer Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Davita Chemicals, Llc
Labeler Code:
78677
Start Marketing Date: [9]
03-07-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 78677-800-02

Package Description: 59 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-04

Package Description: 118 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-06

Package Description: 177 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-08

Package Description: 236 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-10

Package Description: 295 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-12

Package Description: 354 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-16

Package Description: 473 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-24

Package Description: 709 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-32

Package Description: 946 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-64

Package Description: 1892 mL in 1 BOTTLE, DISPENSING

NDC Code 78677-800-70

Package Description: 3785 mL in 1 JUG

NDC Code 78677-800-71

Package Description: 3785 mL in 1 BOX, UNIT-DOSE

NDC Code 78677-800-73

Package Description: 11356 mL in 1 DRUM

NDC Code 78677-800-75

Package Description: 208198 mL in 1 DRUM

NDC Code 78677-800-83

Package Description: 124919 mL in 1 DRUM

NDC Code 78677-800-99

Package Description: 2271247 mL in 1 TANK

Product Details

What is NDC 78677-800?

The NDC code 78677-800 is assigned by the FDA to the product Purevita 80% Hand Sanitizer Gel which is product labeled by Davita Chemicals, Llc. The product's dosage form is . The product is distributed in 16 packages with assigned NDC codes 78677-800-02 59 ml in 1 bottle, dispensing , 78677-800-04 118 ml in 1 bottle, dispensing , 78677-800-06 177 ml in 1 bottle, dispensing , 78677-800-08 236 ml in 1 bottle, dispensing , 78677-800-10 295 ml in 1 bottle, dispensing , 78677-800-12 354 ml in 1 bottle, dispensing , 78677-800-16 473 ml in 1 bottle, dispensing , 78677-800-24 709 ml in 1 bottle, dispensing , 78677-800-32 946 ml in 1 bottle, dispensing , 78677-800-64 1892 ml in 1 bottle, dispensing , 78677-800-70 3785 ml in 1 jug , 78677-800-71 3785 ml in 1 box, unit-dose , 78677-800-73 11356 ml in 1 drum , 78677-800-75 208198 ml in 1 drum , 78677-800-83 124919 ml in 1 drum , 78677-800-99 2271247 ml in 1 tank . 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 Purevita 80% Hand Sanitizer Gel?

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.

Which are Purevita 80% Hand Sanitizer Gel UNII Codes?

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

Which are Purevita 80% Hand Sanitizer Gel 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 Purevita 80% Hand Sanitizer Gel?

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".