NDC 51706-304 Bodycology Moisturizing Hand Sanitizer Midnight Garden

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:
51706-304
Proprietary Name:
Bodycology Moisturizing Hand Sanitizer Midnight Garden
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Landy International
Labeler Code:
51706
Start Marketing Date: [9]
06-30-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 51706-304-02

Package Description: 1 BOTTLE in 1 PACKAGE / 55 mL in 1 BOTTLE (51706-304-01)

Product Details

What is NDC 51706-304?

The NDC code 51706-304 is assigned by the FDA to the product Bodycology Moisturizing Hand Sanitizer Midnight Garden which is product labeled by Landy International. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51706-304-02 1 bottle in 1 package / 55 ml in 1 bottle (51706-304-01). 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 Bodycology Moisturizing Hand Sanitizer Midnight Garden?

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

Which are Bodycology Moisturizing Hand Sanitizer Midnight Garden UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Bodycology Moisturizing Hand Sanitizer Midnight Garden?

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".