warnings
Warnings Keep out of reach of children. In case of overdose get medical help or contact a Poison Control Center right away.
SIMETHICONE INFANT Gas Relief Drops
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
- SIMETHICONE INFANT Gas Relief Drops
- Generic name
- SIMETHICONE
- Manufacturer
- Atlantic Biologicals Corp.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 410d80fc-e55b-08d0-e063-6294a90aba73
- SPL ID
- 4d4f1d08-e4ba-c0bc-e063-6294a90ae949
- Version
- 4
- Effective date
- 2026-03-18
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:45
| 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 | SIMETHICONE INFANT Gas Relief Drops | openfda.brand_name | |
| generic name | SIMETHICONE | openfda.generic_name | |
| manufacturer name | Atlantic Biologicals Corp. | openfda.manufacturer_name | |
| ndc | package | 17856-1017-7 | openfda.package_ndc |
| ndc | package | 17856-1017-4 | openfda.package_ndc |
| ndc | package | 17856-1017-9 | openfda.package_ndc |
| ndc | package | 17856-1017-5 | openfda.package_ndc |
| ndc | package | 17856-1017-3 | openfda.package_ndc |
| ndc | package | 17856-1017-2 | openfda.package_ndc |
| ndc | package | 17856-1017-8 | openfda.package_ndc |
| ndc | package | 17856-1017-1 | openfda.package_ndc |
| ndc | package | 17856-1017-6 | openfda.package_ndc |
| ndc | product | 17856-1017 | openfda.product_ndc |
| ndc11 | package | 17856101709 | derived:openfda.package_ndc |
| ndc11 | package | 17856101708 | derived:openfda.package_ndc |
| ndc11 | package | 17856101707 | derived:openfda.package_ndc |
| ndc11 | package | 17856101705 | derived:openfda.package_ndc |
| ndc11 | package | 17856101703 | derived:openfda.package_ndc |
| ndc11 | package | 17856101702 | derived:openfda.package_ndc |
| ndc11 | package | 17856101704 | derived:openfda.package_ndc |
| ndc11 | package | 17856101706 | derived:openfda.package_ndc |
| ndc11 | package | 17856101701 | derived:openfda.package_ndc |
| rxcui | 198857 | openfda.rxcui | |
| spl id | 4d4f1d08-e4ba-c0bc-e063-6294a90ae949 | id | |
| spl set id | 410d80fc-e55b-08d0-e063-6294a90aba73 | 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.