Home NDC 37808-111 HEB Regular Strength
Product NDC 37808-111
11-digit product format 378080111
Labeler code 37808
Product ID 37808-111_c2e4b102-ef37-4d4b-ba3b-58c5ca8e3048
Type HUMAN OTC DRUG
Nonproprietary name Calcium Carbonate
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler HEB
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-03-06
Substance CALCIUM CARBONATE
Active strength 500 mg/1
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 HEB Regular Strength
Brand name suffix Peppermint Flavor
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM CARBONATE 500 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-111-15 HEB Regular StrengthPeppermint Flavor 150 in 1 BOTTLE, PLASTIC TABLET, CHEWABLE 150 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-111 HEB REGULAR STRENGTH PEPPERMINT FLAVOR (CALCIUM CARBONATE) TABLET, CHEWABLE [HEB] 6 Current NDC, Legacy NDC, 1 package rows 20240915_5f7b4706-674d-425e-9504-820a9704e8da.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 37808-111-15 37808011115 150 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (37808-111-15) 2019-03-06 0000-00-00 No No Current