NDC 34690-5001 Rose Sap Patch

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:
34690-5001
Proprietary Name:
Rose Sap Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kji Industrial Co Ltd
Labeler Code:
34690
Start Marketing Date: [9]
01-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 34690-5001-1

Package Description: 4 g in 1 BOX

NDC Code 34690-5001-2

Package Description: 4 g in 1 BOX

NDC Code 34690-5001-3

Package Description: 4 g in 1 BOX

NDC Code 34690-5001-4

Package Description: 4 g in 1 BOX

Product Details

What is NDC 34690-5001?

The NDC code 34690-5001 is assigned by the FDA to the product Rose Sap Patch which is product labeled by Kji Industrial Co Ltd. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 34690-5001-1 4 g in 1 box , 34690-5001-2 4 g in 1 box , 34690-5001-3 4 g in 1 box , 34690-5001-4 4 g in 1 box . 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 Rose Sap Patch?

DirectionsAdults and children 4 years of age and over:Step 1: Clean and dry area for the patch to be attachedStep 2: Remove the protective cover sheet and gently applyStep 3: Leave it on at least 4 hours before removalChildren under 4 years of age: Consult a doctor

Which are Rose Sap Patch UNII Codes?

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

* 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".