NDC 70380-340 Ultra Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70380 - Miguhara
- 70380-340 - Ultra Whitening
Product Packages
NDC Code 70380-340-01
Package Description: 50 mL in 1 CARTON
Product Details
What is NDC 70380-340?
What are the uses for Ultra Whitening?
Which are Ultra Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
Which are Ultra Whitening 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:
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Ultra Whitening?
- RxCUI: 1093331 - niacinamide 2 % Topical Cream
- RxCUI: 1093331 - niacinamide 20 MG/ML Topical Cream
* 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".