Home NDC 41250-978 Meijer Extra Strength
Product NDC 41250-978
11-digit product format 412500978
Labeler code 41250
Product ID 41250-978_96ee9912-4776-4aa2-a349-400a6b9fea9e
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate ,Magnesium Hydroxide
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler MEIJER DISTRIBUTION INC
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-18
Substance CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Active strength 675; 135 mg/1; mg/1
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Meijer Extra Strength
Brand name suffix Freshmint Flavor
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 675 mg/1 MAGNESIUM HYDROXIDE 135 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-978-10 Meijer Extra StrengthFreshmint Flavor 100 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 100 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-978 MEIJER EXTRA STRENGTH FRESHMINT FLAVOR (CALCIUM CARBONATE ,MAGNESIUM HYDROXIDE) TABLET, CHEWABLE [MEIJER DISTRIBUTION INC] 7 Current NDC, Legacy NDC, 1 package rows 20241019_376665cc-0a2f-4ff7-91bb-be7e476af7a7.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 8 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 41250-978-10 41250097810 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (41250-978-10) 2019-04-18 0000-00-00 No No Current