NDC 66854-023 Spai-sons Marigold Oily Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 66854 - Spai-sons Pharmaceutical International Cosmetics
- 66854-023 - Spai-sons
Product Packages
NDC Code 66854-023-01
Package Description: 9 g in 1 JAR
NDC Code 66854-023-02
Package Description: 33 g in 1 JAR
NDC Code 66854-023-03
Package Description: 60 g in 1 TUBE
Product Details
What is NDC 66854-023?
What are the uses for Spai-sons Marigold Oily Skin?
Which are Spai-sons Marigold Oily Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Spai-sons Marigold Oily Skin 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)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- LACTIC ACID (UNII: 33X04XA5AT)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYSORBATE 85 (UNII: A7F3N56197)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- URTICA DIOICA LEAF (UNII: X6M0DRN46Q)
- SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)
- CHINESE CINNAMON (UNII: WS4CQ062KM)
- GINGER (UNII: C5529G5JPQ)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIMETHICONOL (41 MPA.S) (UNII: 343C7U75XW)
- DIMETHICONE PEG-7 ISOSTEARATE (UNII: JVS3399FNW)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ALLANTOIN (UNII: 344S277G0Z)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".