Home NDC 72559-019 Curist Gas Relief
Product NDC 72559-019
11-digit product format 725590019
Labeler code 72559
Product ID 72559-019_2d566593-1510-ac0d-e063-6294a90a2f22
Type HUMAN OTC DRUG
Nonproprietary name Simethicone
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler Little Pharma, Inc.
Application M002
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-04-07
Substance DIMETHICONE
Active strength 250 mg/1
Pharmacologic classes Skin Barrier Activity [PE]
NDC exclude flag No
Listing certified through 2026-12-31
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 Curist Gas Relief
Brand name suffix Maximum Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE 250 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 92RU3N3Y1O Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 412111 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72559-019-23 Curist Gas ReliefMaximum Strength 300 in 1 BOTTLE CAPSULE, LIQUID FILLED 300 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72559-019 CURIST GAS RELIEF MAXIMUM STRENGTH (SIMETHICONE) CAPSULE, LIQUID FILLED [LITTLE PHARMA, INC.] 5 Current NDC, Legacy NDC, 1 package rows 20250209_dc15a8e6-8924-f5c2-e053-2a95a90ab2c0.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 13 · 255 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 72559-019-23 72559001923 300 CAPSULE, LIQUID FILLED in 1 BOTTLE (72559-019-23) 2022-04-07 0000-00-00 No No Current