NDC 53010-2001 Jnh Magic Bb
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Get all the details for National Drug Code (NDC) 53010-2001 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 53010-2001?
What are the uses for Jnh Magic Bb?
Which are Jnh Magic Bb UNII Codes?
The UNII codes for the active ingredients in this product are:
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H) (Active Moiety)
Which are Jnh Magic Bb 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:
- WHEAT GERM (UNII: YR3G369F5A)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)
- ALLANTOIN (UNII: 344S277G0Z)
- HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
- OLEA EUROPAEA FRUIT VOLATILE OIL (UNII: 8E7358CX1J)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
- PAEONIA SUFFRUTICOSA ROOT (UNII: 7M7E9A2C8J)
- CERAMIDE 3 (UNII: 4370DF050B)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- TEA LEAF OIL (UNII: VC855RRT77)
- MICA (UNII: V8A1AW0880)
- CITRUS PARADISI FRUIT OIL (UNII: 6A7N43E0OJ)
- ZANTHOXYLUM PIPERITUM FRUIT PULP (UNII: 7PFC2VA251)
- HYDROLYSED BOVINE COLLAGEN (ENZYMATIC; 2000-5000 MW) (UNII: 5WE8P977RQ)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- OCTYLDODECYL MYRISTATE (UNII: S013N99GR8)
- DIISOSTEARYL MALATE (UNII: QBS8A3XZGQ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- LIMA BEAN (UNII: 112YH1ZMX2)
- MONOSODIUM GLUTAMATE (UNII: W81N5U6R6U)
- PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- SYRINGA VULGARIS FLOWER (UNII: 9V5O040S3W)
- LEVOMENOL (UNII: 24WE03BX2T)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- BUDDLEJA DAVIDII WHOLE (UNII: 8JZ8B2V1OV)
- ZINC STEARATE (UNII: H92E6QA4FV)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- MAGNESIUM SULFATE (UNII: DE08037SAB)
- OLEIC ACID (UNII: 2UMI9U37CP)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- CANANGA ODORATA FLOWER (UNII: 76GTF6Z97M)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".