NDC 71704-002 House Living
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71704 - Guangzhou Beauty Cosmetic Co., Ltd
- 71704-002 - House Living
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?
What are the uses for House Living?
Which are House Living UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
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:
- PEG/PPG-116/66 COPOLYMER (UNII: JP0CK963E0)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM PYROPHOSPHATE DECAHYDRATE (UNII: IY3DKB96QW)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for House Living?
- 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.
[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".