NDC 20276-156 Lucky Instant Hand Sanitizer Citrus Zest

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:
20276-156
Proprietary Name:
Lucky Instant Hand Sanitizer Citrus Zest
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Delta Brands Inc
Labeler Code:
20276
Start Marketing Date: [9]
03-01-2010
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 20276-156-02

Package Description: 2 BOTTLE, SPRAY in 1 BLISTER PACK / 60 mL in 1 BOTTLE, SPRAY (20276-156-60)

NDC Code 20276-156-05

Package Description: 148 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-08

Package Description: 237 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-10

Package Description: 296 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-12

Package Description: 355 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-24

Package Description: 710 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-36

Package Description: 1065 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-40

Package Description: 1183 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-48

Package Description: 1420 mL in 1 BOTTLE, PUMP

NDC Code 20276-156-60

Package Description: 60 mL in 1 BOTTLE, SPRAY

NDC Code 20276-156-64

Package Description: 1893 mL in 1 BOTTLE, PLASTIC

NDC Code 20276-156-85

Package Description: 3785 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 20276-156?

The NDC code 20276-156 is assigned by the FDA to the product Lucky Instant Hand Sanitizer Citrus Zest which is product labeled by Delta Brands Inc. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 20276-156-02 2 bottle, spray in 1 blister pack / 60 ml in 1 bottle, spray (20276-156-60), 20276-156-05 148 ml in 1 bottle, pump , 20276-156-08 237 ml in 1 bottle, pump , 20276-156-10 296 ml in 1 bottle, pump , 20276-156-12 355 ml in 1 bottle, pump , 20276-156-24 710 ml in 1 bottle, pump , 20276-156-36 1065 ml in 1 bottle, pump , 20276-156-40 1183 ml in 1 bottle, pump , 20276-156-48 1420 ml in 1 bottle, pump , 20276-156-60 60 ml in 1 bottle, spray , 20276-156-64 1893 ml in 1 bottle, plastic , 20276-156-85 3785 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 Lucky Instant Hand Sanitizer Citrus Zest?

Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. Recommended for repeated use

Which are Lucky Instant Hand Sanitizer Citrus Zest UNII Codes?

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

Which are Lucky Instant Hand Sanitizer Citrus Zest 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 Lucky Instant Hand Sanitizer Citrus Zest?

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".