NDC 69089-101 Personal Wash Cloths

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:
69089-101
Proprietary Name:
Personal Wash Cloths
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ginni Filaments Limited
Labeler Code:
69089
Start Marketing Date: [9]
07-14-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69089-101-10

Package Description: 10 CLOTH in 1 CARTON

Product Details

What is NDC 69089-101?

The NDC code 69089-101 is assigned by the FDA to the product Personal Wash Cloths which is product labeled by Ginni Filaments Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69089-101-10 10 cloth in 1 carton . 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 Personal Wash Cloths?

Washcloths can be used at room temperature or heated in a microwave for extra comfort. Use one wash cloth for each of the following areas1. Face, Neck, Chest 2. Left and right arm, 3. Perineum, 4.Left and Right leg, 5.Back and ButtocksHeating instructionsPlace full packet in microwave, peel open label approx. 1 inch and heat for 15 seconds, then, follow bathing instructions.(test temperature to avoid burning skin) gloved hands may reduce sensitivity to heat. Check temperature for infants or skin sensitive individualsDo not overheat! Do not reheat.

Which are Personal Wash Cloths UNII Codes?

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

Which are Personal Wash Cloths 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:

* 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".