NDC 69877-026 Vitamin B Complex
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What is NDC 69877-026?
What are the uses for Vitamin B Complex?
Which are Vitamin B Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- RIBOFLAVIN 5'-PHOSPHATE SODIUM (UNII: 20RD1DZH99)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- DEXPANTHENOL (UNII: 1O6C93RI7Z) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- THIAMINE HYDROCHLORIDE (UNII: M572600E5P)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
Which are Vitamin B Complex 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:
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
What is the NDC to RxNorm Crosswalk for Vitamin B Complex?
- RxCUI: 801177 - dexpanthenol 2 MG/ML / niacinamide 100 MG/ML / riboflavin 2 MG/ML / thiamine 100 MG/ML / vitamin B6 2 MG/ML Injectable Solution
- RxCUI: 801177 - dexpanthenol 2 MG / niacinamide 100 MG / pyridoxine 2 MG / riboflavin 2 MG / thiamine 100 MG per ML Injectable Solution
- RxCUI: 801177 - dexpanthenol 2 MG/ML / Niacinamide 100 MG/ML / Riboflavin 2 MG/ML / vitamin B1 100 MG/ML / Vitamin B6 2 MG/ML Injectable Solution
- RxCUI: 801177 - dexpanthenol 2 MG/ML / Niacinamide 100 MG/ML / Riboflavin 2 MG/ML / vit-B1 100 MG/ML / Vitamin B6 2 MG/ML Injectable Solution
- RxCUI: 801177 - vitamin B complex Injectable Solution
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[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".