NDC 70518-2971 Fexofenadine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70518 - Remedyrepack Inc.
- 70518-2971 - Fexofenadine Hydrochloride
Product Characteristics
Product Packages
NDC Code 70518-2971-0
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 70518-2971-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 70518-2971?
What are the uses for Fexofenadine Hydrochloride?
Which are Fexofenadine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- FEXOFENADINE HYDROCHLORIDE (UNII: 2S068B75ZU)
- FEXOFENADINE (UNII: E6582LOH6V) (Active Moiety)
Which are Fexofenadine Hydrochloride 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Fexofenadine Hydrochloride?
- RxCUI: 997420 - fexofenadine HCl 180 MG 24 HR Oral Tablet
- RxCUI: 997420 - fexofenadine hydrochloride 180 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Fexofenadine
Fexofenadine is used to relieve the allergy symptoms of seasonal allergic rhinitis (''hay fever''), including runny nose; sneezing; red, itchy, or watery eyes; or itching of the nose, throat, or roof of the mouth in adults and children 2 years of age and older. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash in adults and children 6 months of age and older. Fexofenadine is in a class of medications called antihistamines. It works by blocking the effects of histamine, a substance in the body that causes allergy symptoms.
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* Please review the disclaimer below.
[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".