NDC 69579-103 P1p Skin Rebirth Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 69579-103?
Which are P1p Skin Rebirth Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
Which are P1p Skin Rebirth Cream 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TOTAROL (UNII: 67NH2854WW)
- BATILOL (UNII: 39YR661C4U)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- ARGININE (UNII: 94ZLA3W45F)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ISODODECANE (UNII: A8289P68Y2)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- LAURYL TRISILOXANE (UNII: 5OHO78HI1D)
- CITRUS PARADISI SEED (UNII: 12F08874Y7)
- ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)
- OCTANEDIOL (UNII: 806K32R50Z)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- ACEGLUTAMIDE (UNII: 01J18G9G97)
- NEPIDERMIN (UNII: TZK30RF92W)
- MECASERMIN (UNII: 7GR9I2683O)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
- FIBROBLAST GROWTH FACTOR-1 (UNII: G53298VN9Y)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".