warnings
Warnings
CVS PHARMACY Extra Strength Gas Relief
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
- CVS PHARMACY Extra Strength Gas Relief
- Generic name
- SIMETHICONE ANTIGAS
- Manufacturer
- CVS
- Product type
- HUMAN OTC DRUG
- SPL set ID
- b0fc2f24-cd63-4bb2-b9bb-a73449bcc169
- SPL ID
- 078cc154-b97f-4843-a119-22283d31560f
- Version
- 6
- Effective date
- 2026-08-13
- 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 02:16:48
| 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 | CVS PHARMACY Extra Strength Gas Relief | openfda.brand_name | |
| generic name | SIMETHICONE ANTIGAS | openfda.generic_name | |
| manufacturer name | CVS | openfda.manufacturer_name | |
| ndc | package | 51316-011-18 | openfda.package_ndc |
| ndc | product | 51316-011 | openfda.product_ndc |
| ndc11 | package | 51316001118 | derived:openfda.package_ndc |
| rxcui | 314221 | openfda.rxcui | |
| spl id | 078cc154-b97f-4843-a119-22283d31560f | id | |
| spl set id | b0fc2f24-cd63-4bb2-b9bb-a73449bcc169 | 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.