NDC 61722-277 Flormar Smooth Touch Foundation 08 Medium Beige
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61722 - Kosan Kozmetik Sanayi Ve Ticaret A.s.
- 61722-277 - Flormar Smooth Touch Foundation 08 Medium Beige
Product Packages
NDC Code 61722-277-00
Package Description: 1 TUBE in 1 BOX / 30 mL in 1 TUBE
Product Details
What is NDC 61722-277?
What are the uses for Flormar Smooth Touch Foundation 08 Medium Beige?
Which are Flormar Smooth Touch Foundation 08 Medium Beige UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Flormar Smooth Touch Foundation 08 Medium Beige 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- UREA (UNII: 8W8T17847W)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- TREHALOSE (UNII: B8WCK70T7I)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- CYMBIDIUM HOOKERIANUM FLOWER (UNII: H2DJ03DI5I)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FIG (UNII: TGD87RII2U)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".