NDC 70569-840 Gialax
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70569-840?
Which are Gialax UNII Codes?
The UNII codes for the active ingredients in this product are:
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P) (Active Moiety)
Which are Gialax 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:
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- CALCIUM SILICATE (UNII: S4255P4G5M)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- MONOPOTASSIUM PHOSPHITE (UNII: 59RSS63D8J)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PIGMENT BLUE 1 (UNII: 4SBE571RQF)
- ASPARTAME (UNII: Z0H242BBR1)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POTASSIUM CITRATE (UNII: EE90ONI6FF)
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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".