NDC 47649-1301 Dr.whitiss 35%
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 47649 - Nibec Co., Ltd
- 47649-1301 - Dr.whitiss 35%
Product Packages
NDC Code 47649-1301-2
Package Description: 4 SYRINGE in 1 PACKAGE / 1 g in 1 SYRINGE (47649-1301-1)
Product Details
What is NDC 47649-1301?
What are the uses for Dr.whitiss 35%?
Which are Dr.whitiss 35% UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARBAMIDE PEROXIDE (UNII: 31PZ2VAU81)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V) (Active Moiety)
Which are Dr.whitiss 35% 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:
- POVIDONE K90 (UNII: RDH86HJV5Z)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
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[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".