NDC 73321-001 Two Step Jelly Mask - Brightening And Nutrition
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73321 - Dpark Corporation
- 73321-001 - Two Step Jelly Mask - Brightening And Nutrition
Product Packages
NDC Code 73321-001-02
Package Description: 5 POUCH in 1 CARTON / 1.5 mL in 1 POUCH (73321-001-01)
Product Details
What is NDC 73321-001?
What are the uses for Two Step Jelly Mask - Brightening And Nutrition?
Which are Two Step Jelly Mask - Brightening And Nutrition UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Two Step Jelly Mask - Brightening And Nutrition 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)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
- GLYCERIN (UNII: PDC6A3C0OX)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- ALCOHOL (UNII: 3K9958V90M)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PAEONIA X SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CHAMOMILE (UNII: FGL3685T2X)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
What is the NDC to RxNorm Crosswalk for Two Step Jelly Mask - Brightening And Nutrition?
- RxCUI: 2197846 - salicylic acid 0.01 % Topical Swab
- RxCUI: 2197846 - salicylic acid 0.1 MG/ML Medicated Pad
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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".