NDC 53009-1001 Mioggi Healing Effector Rx Collagenic
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 53009-1001?
What are the uses for Mioggi Healing Effector Rx Collagenic?
Which are Mioggi Healing Effector Rx Collagenic UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are Mioggi Healing Effector Rx Collagenic 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:
- SHEA BUTTER (UNII: K49155WL9Y)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYETHYLENE GLYCOL 11000 (UNII: R0XY39567G)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- MACADAMIA NUT (UNII: Y5432RGW8N)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SQUALANE (UNII: GW89575KF9)
- GLYCERIN (UNII: PDC6A3C0OX)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".