Home NDC 37808-231-30 HEB Anti Gas
Product NDC 37808-231
Requested package NDC 37808-231-30
11-digit product format 378080231
Labeler code 37808
Product ID 37808-231_403f76f6-9d3e-53a9-e063-6294a90a3775
Type HUMAN OTC DRUG
Nonproprietary name Simethicone
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler HEB
Application M002
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-18
Substance DIMETHICONE, UNSPECIFIED
Active strength 125 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 2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 37808-231 37808-231-30 I Inactivated by FDA excluded / ndc_excluded.zip 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 37808-231 37808-231-30 I Inactivated by FDA excluded / ndc_excluded.zip 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 37808-231 37808-231-30 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base HEB Anti Gas
Brand name suffix Extra Strength
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE, UNSPECIFIED 125 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 198852 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 37808-231-20 HEB Anti GasExtra Strength 30 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 30 8 37808-231-20 HEB Anti GasExtra Strength 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 8 37808-231-30 HEB Anti GasExtra Strength 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 8 37808-231-30 HEB Anti GasExtra Strength 200 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 200 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-231 HEB ANTI GAS EXTRA STRENGTH (SIMETHICONE) CAPSULE, LIQUID FILLED [HEB] 7 Current NDC, Legacy NDC, 4 package rows 20240621_71f901c6-b5a4-4115-98f2-628e0b79d7ac.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 · 258 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 37808-231-30 37808023130 2 BLISTER PACK in 1 CARTON (37808-231-30) / 200 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2019-04-18 0000-00-00 No No Current