NDC 70367-010 Soothing Antiseptic Mask With Sulfur
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70367 - Only Yourx, Inc.
- 70367-010 - Soothing Antiseptic Mask With Sulfur
Product Characteristics
Product Packages
NDC Code 70367-010-01
Package Description: 30 mL in 1 TUBE
NDC Code 70367-010-04
Package Description: 120 mL in 1 TUBE
NDC Code 70367-010-08
Package Description: 240 mL in 1 TUBE
Product Details
What is NDC 70367-010?
What are the uses for Soothing Antiseptic Mask With Sulfur?
Which are Soothing Antiseptic Mask With Sulfur UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Soothing Antiseptic Mask With Sulfur 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- WATER (UNII: 059QF0KO0R)
- KAOLIN (UNII: 24H4NWX5CO)
- BENTONITE (UNII: A3N5ZCN45C)
- GLYCERIN (UNII: PDC6A3C0OX)
- 2-(1-CHLOROCYCLOPROPYL)-3-(2-CHLOROPHENYL)-1,2-PROPANEDIOL (UNII: SJ211700DZ)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Soothing Antiseptic Mask With Sulfur?
- 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".