NDC 69871-003 Obeo 7way Moisture
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69871-003?
What are the uses for Obeo 7way Moisture?
Which are Obeo 7way Moisture UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Obeo 7way Moisture 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)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TROLAMINE (UNII: 9O3K93S3TK)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SHEA BUTTER (UNII: K49155WL9Y)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PROPANEDIOL (UNII: 5965N8W85T)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- IMPERATA CYLINDRICA ROOT (UNII: VYT2JA85NH)
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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".