NDC 90069-205 Purpleu Baobab Rejuvenating Ampoule
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 90069-205 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.
Code Structure Chart
Product Details
What is NDC 90069-205?
What are the uses for Purpleu Baobab Rejuvenating Ampoule?
Which are Purpleu Baobab Rejuvenating Ampoule UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE (UNII: K72T3FS567)
- ADENOSINE (UNII: K72T3FS567) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
Which are Purpleu Baobab Rejuvenating Ampoule 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:
- GARLIC (UNII: V1V998DC17)
- PSIDIUM GUAJAVA LEAF (UNII: PM0F263X0Y)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- HIBISCUS SABDARIFFA FLOWER (UNII: 45TGG6IU6M)
- JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- MENTHA X ROTUNDIFOLIA LEAF (UNII: K59TXG2L3U)
- HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
- 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CHOLETH-24 (UNII: 5UE7I54O43)
- TROMETHAMINE (UNII: 023C2WHX2V)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- HYALURONIC ACID (UNII: S270N0TRQY)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- PROPANEDIOL (UNII: 5965N8W85T)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV)
- ALLANTOIN (UNII: 344S277G0Z)
- CERAMIDE 3 (UNII: 4370DF050B)
- MADECASSOSIDE (UNII: CQ2F5O6YIY)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47)
- TETRADECYL AMINOBUTYROYLVALYLAMINOBUTYRIC UREA TRIFLUOROACETATE (UNII: 0UBP26S1LG)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LUFFA AEGYPTIACA FRUIT (UNII: QKL9NEO1F9)
- GUAVA (UNII: 74O70D6VG0)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- ORANGE OIL (UNII: AKN3KSD11B)
- WATER (UNII: 059QF0KO0R)
- ADANSONIA DIGITATA FRUIT (UNII: 51N9TR1W6P)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- ALCOHOL (UNII: 3K9958V90M)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- SUGARCANE (UNII: 81H2R5AOH3)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".