warnings
Warnings If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
Gas Relief Extra Strength
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Gas Relief Extra Strength
- Generic name
- SIMETHICONE
- Manufacturer
- H E B
- Product type
- HUMAN OTC DRUG
- SPL set ID
- c153585f-0f44-40ad-8246-5d9edae8325e
- SPL ID
- dd0b9f77-06e9-4eca-bc6d-4a6c57a62e15
- Version
- 5
- Effective date
- 2026-04-02
- Source export date
- 2026-10-12
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:13:34
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M002 | openfda.application_number | |
| brand name | Gas Relief Extra Strength | openfda.brand_name | |
| generic name | SIMETHICONE | openfda.generic_name | |
| manufacturer name | H E B | openfda.manufacturer_name | |
| ndc | package | 37808-797-10 | openfda.package_ndc |
| ndc | product | 37808-797 | openfda.product_ndc |
| ndc11 | package | 37808079710 | derived:openfda.package_ndc |
| rxcui | 198852 | openfda.rxcui | |
| spl id | dd0b9f77-06e9-4eca-bc6d-4a6c57a62e15 | id | |
| spl set id | c153585f-0f44-40ad-8246-5d9edae8325e | set_id | |
| unii | 92RU3N3Y1O | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.