NDC 66273-0002 Exence White
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66273 - Aquimpex Spa
- 66273-0002 - Exence White
Product Packages
NDC Code 66273-0002-2
Package Description: 12 BOTTLE, PLASTIC in 1 BOX / 500 mL in 1 BOTTLE, PLASTIC (66273-0002-1)
Product Details
What is NDC 66273-0002?
Which are Exence White UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Exence White 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:
- WATER (UNII: 059QF0KO0R)
- ROSEMARY (UNII: IJ67X351P9)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER 934 (UNII: Z135WT9208)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- BRASSICA RAPA VAR. RAPA OIL (UNII: N4G8379626)
What is the NDC to RxNorm Crosswalk for Exence White?
- RxCUI: 153031 - hydroquinone 2 % Topical Cream
- RxCUI: 153031 - hydroquinone 20 MG/ML Topical Cream
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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".