Home NDC 21130-717-06 Ultra Strength Gas Relief
Product NDC 21130-717
Requested package NDC 21130-717-06
11-digit product format 211300717
Labeler code 21130
Product ID 21130-717_2df04265-4a90-8001-e063-6294a90afcaa
Type HUMAN OTC DRUG
Nonproprietary name Simethicone
Dosage form CAPSULE
Route ORAL
Labeler BETTER LIVING BRANDS, LLC
Application M002
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-05-20
Substance DIMETHICONE
Active strength 180 mg/1
Pharmacologic classes Skin Barrier Activity [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 3 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 21130-717 21130-717-06 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 21130-717 21130-717-06 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 21130-717 21130-717-06 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Additional Listing Data#
Finished product Yes
Brand name base Ultra Strength Gas Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE 180 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 252294 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21130-717-06 Ultra Strength Gas Relief 60 in 1 BOTTLE CAPSULE 60 3 21130-717-06 Ultra Strength Gas Relief 1 in 1 CARTON CAPSULE 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21130-717 ULTRA STRENGTH GAS RELIEF (SIMETHICONE) CAPSULE [BETTER LIVING BRANDS, LLC] 3 Current NDC, 2 package rows 20250214_eb4bef2c-15dd-434a-e053-2a95a90a616f.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 · 260 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 21130-717-06 21130071706 1 BOTTLE in 1 CARTON (21130-717-06) / 60 CAPSULE in 1 BOTTLE 1 bottle 2023-05-20 No No Current