NDC 11673-106 Up And Up Childrens All Day Allergy Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11673 - Target Corporation
- 11673-106 - Up And Up
Product Characteristics
Product Packages
NDC Code 11673-106-08
Package Description: 1 BOTTLE in 1 CARTON / 120 mL in 1 BOTTLE
Product Details
What is NDC 11673-106?
What are the uses for Up And Up Childrens All Day Allergy Relief?
Which are Up And Up Childrens All Day Allergy Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA)
- CETIRIZINE (UNII: YO7261ME24) (Active Moiety)
Which are Up And Up Childrens All Day Allergy Relief 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:
- ACETIC ACID (UNII: Q40Q9N063P)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM ACETATE ANHYDROUS (UNII: NVG71ZZ7P0)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Up And Up Childrens All Day Allergy Relief?
- RxCUI: 1014673 - cetirizine HCl 5 MG in 5 mL Oral Solution
- RxCUI: 1014673 - cetirizine hydrochloride 1 MG/ML Oral Solution
- RxCUI: 1014673 - cetirizine HCl 1 MG/ML Oral Syrup
- RxCUI: 1014673 - cetirizine HCl 5 MG per 5 ML Oral Solution
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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".