Home NDC 68016-807 Premier Value Nausea Control
Product NDC 68016-807
11-digit product format 680160807
Labeler code 68016
Product ID 68016-807_eeb45790-8ef7-4d27-b114-dcd78215ff47
Type HUMAN OTC DRUG
Nonproprietary name dextrose(glucose),Levulose(fructose),Phosphoric acid
Dosage form SOLUTION
Route ORAL
Labeler PHARMACY VALUE ALLIANCE, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-04-16
Substance DEXTROSE, UNSPECIFIED FORM; FRUCTOSE; PHOSPHORIC ACID
Active strength 1.87; 1.87; 21.5 g/5mL; g/5mL; mg/5mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Premier Value Nausea Control
Brand name suffix Cherry Flavor
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DEXTROSE, UNSPECIFIED FORM 1.87 g/5mL FRUCTOSE 1.87 g/5mL PHOSPHORIC ACID 21.5 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination IY9XDZ35W2 Internal UNII lookup 6YSS42VSEV Internal UNII lookup E4GA8884NN Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 318146 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68016-807-04 Premier Value Nausea ControlCherry Flavor 1 in 1 CARTON SOLUTION 1 6 68016-807-04 Premier Value Nausea ControlCherry Flavor 118 mL in 1 BOTTLE SOLUTION 118 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68016-807 PREMIER VALUE NAUSEA CONTROL CHERRY FLAVOR (DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID) SOLUTION [PHARMACY VALUE ALLIANCE, LLC] 6 Current NDC, Legacy NDC, 2 package rows 20241030_8f000438-a9c3-45ca-8cb5-79151b2b3ead.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68016-807-04 68016080704 1 BOTTLE in 1 CARTON (68016-807-04) / 118 mL in 1 BOTTLE 1 bottle 2019-04-16 0000-00-00 No No Current