NDC 17856-0091 Aluminum Hydroxide
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17856-0091?
What are the uses for Aluminum Hydroxide?
Which are Aluminum Hydroxide UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (Active Moiety)
Which are Aluminum Hydroxide 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)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Aluminum Hydroxide?
- RxCUI: 308078 - aluminum hydroxide 320 MG in 5 mL Oral Suspension
- RxCUI: 308078 - aluminum hydroxide 64 MG/ML Oral Suspension
- RxCUI: 308078 - aluminum hydroxide 320 MG per 5 ML Oral Suspension
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Patient Education
Aluminum Hydroxide
Aluminum hydroxide is used for the relief of heartburn, sour stomach, and peptic ulcer pain and to promote the healing of peptic ulcers.
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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".