NDC 69779-001 Blood Sugar
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69779-001?
What are the uses for Blood Sugar?
Which are Blood Sugar UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- CARPINUS BETULUS FLOWER (UNII: 07YL55QKZ9)
- CARPINUS BETULUS FLOWER (UNII: 07YL55QKZ9) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
- SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
Which are Blood Sugar 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:
- AMERICAN GINSENG (UNII: 8W75VCV53Q)
- APRICOT (UNII: 269CJD5GZ9)
- JERUSALEM ARTICHOKE (UNII: R6PI58X44M)
- MELISSA OFFICINALIS FLOWERING TOP (UNII: 5JQG17B06J)
- NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
- PUNICA GRANATUM FLOWER (UNII: D9B634V4GP)
- WATER (UNII: 059QF0KO0R)
- BETA VULGARIS (UNII: 4G174V5051)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
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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".