NDC 42851-089 Zo Skin Health Sulfur Masque
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42851 - Zo Skin Health, Inc.
- 42851-089 - Zo Skin Health Sulfur Masque
Product Details
What is NDC 42851-089?
What are the uses for Zo Skin Health Sulfur Masque?
Which are Zo Skin Health Sulfur Masque UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Zo Skin Health Sulfur Masque 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)
- TALC (UNII: 7SEV7J4R1U)
- KAOLIN (UNII: 24H4NWX5CO)
- GLYCERIN (UNII: PDC6A3C0OX)
- BENTONITE (UNII: A3N5ZCN45C)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
What is the NDC to RxNorm Crosswalk for Zo Skin Health Sulfur Masque?
- RxCUI: 1053330 - sulfur 10 % Medicated Liquid Soap
- RxCUI: 1053330 - sulfur 100 MG/ML Medicated Liquid Soap
- RxCUI: 1053330 - sulfur 10 % Topical Mask
* 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".