NDC 71704-002 House Living

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:
71704-002
Proprietary Name:
House Living
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guangzhou Beauty Cosmetic Co., Ltd
Labeler Code:
71704
Start Marketing Date: [9]
07-10-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71704-002-01

Package Description: 24 TUBE in 1 CARTON / 113 g in 1 TUBE

Product Details

What is NDC 71704-002?

The NDC code 71704-002 is assigned by the FDA to the product House Living which is product labeled by Guangzhou Beauty Cosmetic Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71704-002-01 24 tube in 1 carton / 113 g in 1 tube. 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 House Living?

Adults and children 2 years of age and older:brush teeth thoroughly, preferably after meals or at least twice a day or use as directed by a dentist or doctor.instruct children 6 years of age in good brushing and rinsing habits(to minimize swallowing)suprevise children as necessary untill capable of using without supervision.children under 2 years of age :consult a dentist or doctor

Which are House Living UNII Codes?

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

Which are House Living 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 House Living?

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:
  • RxCUI: 1038841 - potassium nitrate 5 % / sodium fluoride 0.15 % Toothpaste
  • RxCUI: 1038841 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste
  • RxCUI: 1038841 - pot nitrate 0.05 MG/MG / sodium fluoride 0.0015 MG/MG gel Toothpaste
  • RxCUI: 1038841 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0015 MG/MG Toothpaste

* 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".