NDC 0178-0832 Citranatal B-calm
Ascorbic Acid,Calcium Citrate,Iron,Cholecalciferol,Pyridoxine Hydrochloride,And Folic Acid - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ROUND (C48348)
6 MM
B;6
Code Structure Chart
Product Details
What is NDC 0178-0832?
What are the uses for Citranatal B-calm?
Which are Citranatal B-calm UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- CALCIUM CITRATE (UNII: MLM29U2X85)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- IRON (UNII: E1UOL152H7)
- IRON (UNII: E1UOL152H7) (Active Moiety)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- CHOLECALCIFEROL (UNII: 1C6V77QF41) (Active Moiety)
Which are Citranatal B-calm 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:
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- IRON PENTACARBONYL (UNII: 6WQ62TAQ6Z)
- MAGNESIUM SILICATE (UNII: 9B9691B2N9)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH)
What is the NDC to RxNorm Crosswalk for Citranatal B-calm?
- RxCUI: 1100262 - ascorbic acid 120 MG / calcium citrate 125 MG / cholecalciferol 400 UNT / folic acid 1 MG / iron carbonyl 20 MG / pyridoxine hydrochloride 25 MG Oral Tablet
- RxCUI: 1100262 - calcium citrate 125 MG / folic acid 1 MG / iron carbonyl 20 MG / vitamin B6 25 MG / vitamin C 120 MG / vitamin D3 400 UNT Oral Tablet
- RxCUI: 1100262 - vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / folate 1 MG / Iron Carbonyl 20 MG / vitamin B6 Hydrochloride 25 MG Oral Tablet
- RxCUI: 1100262 - vitamin C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / folate 1 MG / Iron Carbonyl 20 MG / vit-B6 Hydrochloride 25 MG Oral Tablet
- RxCUI: 1100262 - vit-C 120 MG / Calcium Citrate 125 MG / Cholecalciferol 400 UNT / folate 1 MG / Iron Carbonyl 20 MG / vitamin B6 Hydrochloride 25 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Pyridoxine
Pyridoxine, vitamin B6, is required by your body for utilization of energy in the foods you eat, production of red blood cells, and proper functioning of nerves. It is used to treat and prevent vitamin B6 deficiency resulting from poor diet, certain medications, and some medical conditions. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[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 ("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".