NDC 71364-003 Botanic Twenty Light Watery
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71364 - Ritzy Noble Co., Ltd.
- 71364-003 - Botanic Twenty
Product Packages
NDC Code 71364-003-02
Package Description: 1 JAR in 1 BOX / 50 mL in 1 JAR (71364-003-01)
Product Details
What is NDC 71364-003?
What are the uses for Botanic Twenty Light Watery?
Which are Botanic Twenty Light Watery 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 Light Watery 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:
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- ARTEMISIA ANNUA WHOLE (UNII: 58296FW9ZD)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- 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)
- ASPARAGUS COCHINCHINENSIS WHOLE (UNII: 36L6R7F7P9)
- HOUTTUYNIA CORDATA TOP (UNII: 3E4MG0DM0M)
- ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
* Please review the disclaimer below.
[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".