NDC 66854-001 Spai-sons Calendula/marigold
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 66854-001?
What are the uses for Spai-sons Calendula/marigold?
Which are Spai-sons Calendula/marigold UNII Codes?
The UNII codes for the active ingredients in this product are:
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Spai-sons Calendula/marigold 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)
- LACTIC ACID (UNII: 33X04XA5AT)
- DEXTROSE (UNII: IY9XDZ35W2)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- CHAMOMILE (UNII: FGL3685T2X)
- TROLAMINE (UNII: 9O3K93S3TK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- 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".