NDC 71364-101 Botanic Twenty Hypercare Essence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 71364-101 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 71364-101?
What are the uses for Botanic Twenty Hypercare Essence?
Which are Botanic Twenty Hypercare Essence 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 Botanic Twenty Hypercare Essence 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:
- BETAINE (UNII: 3SCV180C9W)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- ARTEMISIA ANNUA WHOLE (UNII: 58296FW9ZD)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- ARGININE (UNII: 94ZLA3W45F)
- COPTIS JAPONICA ROOT (UNII: JH0SWT16D1)
- CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LEPIDIUM MEYENII ROOT (UNII: HP7119212T)
- AUREOBASIDIUM PULLULANS VAR. PULLUTANS (UNII: D1A2NG69CK)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)
- CORYDALIS TURTSCHANINOVII WHOLE (UNII: I94Q8D25FS)
- ILLICIUM VERUM WHOLE (UNII: 52JDS841PX)
- LARIX SIBIRICA WOOD (UNII: KSC3PGF73L)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
- PINUS PINASTER WOOD (UNII: 0L1DQ35D6G)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- ROSMARINUS OFFICINALIS FLOWERING TOP OIL (UNII: OXN0D3N28L)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
- ROSMARINUS OFFICINALIS WHOLE (UNII: EA3289138M)
- BELLIS PERENNIS FLOWER (UNII: 26I94X9A1K)
- FREESIA ALBA FLOWER (UNII: 33X293N6JT)
- LEONTOPODIUM ALPINUM (UNII: 7R4LQP52DM)
- LILIUM CANDIDUM FLOWER (UNII: COV655U2CJ)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0)
- MAGNOLIA LILIIFLORA FLOWER (UNII: SVM28292LH)
- PUNICA GRANATUM SEED (UNII: 7294Z34NS7)
- EDETIC ACID (UNII: 9G34HU7RV0)
- SAUSSUREA INVOLUCRATA FLOWERING TOP (UNII: 65D06L9K7F)
- ASPARAGUS COCHINCHINENSIS WHOLE (UNII: 36L6R7F7P9)
- HOUTTUYNIA CORDATA TOP (UNII: 3E4MG0DM0M)
- ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ALLANTOIN (UNII: 344S277G0Z)
* 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".