Home NDC 41250-495-04 Meijer Anti Nausea
Product NDC 41250-495
Requested package NDC 41250-495-04
11-digit product format 412500495
Labeler code 41250
Product ID 41250-495_41f2495b-ab4e-e0c8-e063-6394a90a5a6b
Type HUMAN OTC DRUG
Nonproprietary name Dextrose(glucose),Levulose(fructose),Phosphoric acid
Dosage form LIQUID
Route ORAL
Labeler MEIJER DISTRIBUTION, INC.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2020-06-29
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 Meijer Anti Nausea
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 41250-495-04 Meijer Anti Nausea 118 mL in 1 BOTTLE LIQUID 118 7 41250-495-04 Meijer Anti Nausea 1 in 1 CARTON LIQUID 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-495 MEIJER ANTI NAUSEA (DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID) LIQUID [MEIJER DISTRIBUTION, INC.] 6 Current NDC, Legacy NDC, 2 package rows 20241020_c3cae237-54e1-4b42-a871-bd497229fe90.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 41250-495-04 41250049504 1 BOTTLE in 1 CARTON (41250-495-04) / 118 mL in 1 BOTTLE 1 bottle 2020-06-29 0000-00-00 No No Current