NDC 71167-002 White-glo 2in1 With Mouthwash
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71167 - Huaian Zongheng Bio-tech Co., Ltd
- 71167-002 - White-glo 2in1 With Mouthwash
Product Packages
NDC Code 71167-002-01
Package Description: 24 TUBE in 1 BOX / 150 g in 1 TUBE
NDC Code 71167-002-02
Package Description: 48 TUBE in 1 BOX / 150 g in 1 TUBE
Product Details
What is NDC 71167-002?
What are the uses for White-glo 2in1 With Mouthwash?
Which are White-glo 2in1 With Mouthwash UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are White-glo 2in1 With Mouthwash 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:
- CHONDRUS CRISPUS (UNII: OQS23HUA1X)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SORBITOL (UNII: 506T60A25R)
- SODIUM SILICATE (UNII: IJF18F77L3)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- POTASSIUM SODIUM SACCHARATE (UNII: 73U34YC90U)
- ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)
- ALCOHOL (UNII: 3K9958V90M)
What is the NDC to RxNorm Crosswalk for White-glo 2in1 With Mouthwash?
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )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".