NDC 61715-131 Milk Of Magnesia
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61715 - Kinray Llc
- 61715-131 - Milk Of Magnesia
Product Characteristics
Product Packages
NDC Code 61715-131-04
Package Description: 355 mL in 1 BOTTLE
Product Details
What is NDC 61715-131?
What are the uses for Milk Of Magnesia?
Which are Milk Of Magnesia UNII Codes?
The UNII codes for the active ingredients in this product are:
- MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- HYDROXIDE ION (UNII: 9159UV381P) (Active Moiety)
Which are Milk Of Magnesia 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:
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- GLYCERIN (UNII: PDC6A3C0OX)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM HYPOCHLORITE (UNII: DY38VHM5OD)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Milk Of Magnesia?
- RxCUI: 253017 - magnesium hydroxide 1200 MG in 15 mL Oral Suspension
- RxCUI: 253017 - magnesium hydroxide 80 MG/ML Oral Suspension
- RxCUI: 253017 - magnesium hydroxide 1200 MG per 15 ML Oral Suspension
- RxCUI: 253017 - milk of magnesia 2400 MG per 30 ML Oral Suspension
- RxCUI: 253017 - milk of magnesia 400 MG per 5 ML Oral Suspension
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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".