NDC 66854-024 Feix Facial
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66854 - Spai-sons Pharmaceutical International Cosmetics
- 66854-024 - Feix
Product Packages
NDC Code 66854-024-01
Package Description: 280 mL in 1 BOTTLE
Product Details
What is NDC 66854-024?
What are the uses for Feix Facial?
Which are Feix Facial UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- DIPYRITHIONE (UNII: 9L87N86R9A)
- DIPYRITHIONE (UNII: 9L87N86R9A) (Active Moiety)
Which are Feix Facial 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCO DIETHANOLAMIDE (UNII: 92005F972D)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- GINGER (UNII: C5529G5JPQ)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- COCO GLUCOSIDE (UNII: ICS790225B)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CHAMOMILE (UNII: FGL3685T2X)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- TRICLOSAN (UNII: 4NM5039Y5X)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- TROLAMINE (UNII: 9O3K93S3TK)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
* 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".