NDC 66854-002 Feix Bioazufre / Biosulphur
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66854 - Spai-sons Phamaceutical International Cosmetics
- 66854-002 - Feix
Product Characteristics
Product Packages
NDC Code 66854-002-01
Package Description: 70 g in 1 BOX
Product Details
What is NDC 66854-002?
What are the uses for Feix Bioazufre / Biosulphur?
Which are Feix Bioazufre / Biosulphur UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Feix Bioazufre / Biosulphur 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:
- SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
- SODIUM PALMITATE (UNII: JQ43KP6296)
- SODIUM STEARATE (UNII: QU7E2XA9TG)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM SARCOSINATE (UNII: 6EHN3PQL8Z)
- PARAFFIN (UNII: I9O0E3H2ZE)
- SODIUM COCOATE (UNII: R1TQH25F4I)
- SODIUM ISETHIONATE (UNII: 3R36J71C17)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIPYRITHIONE (UNII: 9L87N86R9A)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
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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".