warnings
Warnings Allergy alert: Do not use if you have ever had a rash or other allergic reaction to loperamide HCl Heart alert: Taking more than directed can cause serious heart problems or death
Loperamide Hydrochloride and Simethicone
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
- Loperamide Hydrochloride and Simethicone
- Generic name
- LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE
- Manufacturer
- Aurohealth LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 9dd3a6d6-9fff-45b3-8e76-57bf5ee2e07f
- SPL ID
- f2788da1-1ef1-4db9-8271-e786cc2ddd9e
- Version
- 5
- Effective date
- 2025-01-07
- Source export date
- 2026-10-27
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/55ffdfed5c29f1b4aed512886bd3fb7831e157cc4948137779971a558752ed2b/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:07:19
| 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 applno | ANDA | 211059 | derived:openfda.application_number |
| application number | ANDA211059 | openfda.application_number | |
| brand name | Loperamide Hydrochloride and Simethicone | openfda.brand_name | |
| generic name | LOPERAMIDE HYDROCHLORIDE AND SIMETHICONE | openfda.generic_name | |
| manufacturer name | Aurohealth LLC | openfda.manufacturer_name | |
| ndc | package | 58602-815-74 | openfda.package_ndc |
| ndc | package | 58602-815-75 | openfda.package_ndc |
| ndc | package | 58602-815-80 | openfda.package_ndc |
| ndc | package | 58602-815-76 | openfda.package_ndc |
| ndc | product | 58602-815 | openfda.product_ndc |
| ndc11 | package | 58602081575 | derived:openfda.package_ndc |
| ndc11 | package | 58602081580 | derived:openfda.package_ndc |
| ndc11 | package | 58602081574 | derived:openfda.package_ndc |
| ndc11 | package | 58602081576 | derived:openfda.package_ndc |
| rxcui | 978001 | openfda.rxcui | |
| spl id | f2788da1-1ef1-4db9-8271-e786cc2ddd9e | id | |
| spl set id | 9dd3a6d6-9fff-45b3-8e76-57bf5ee2e07f | set_id | |
| unii | 77TI35393C | openfda.unii | |
| 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.