warnings
Warnings
Premier Value Maximum 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
- Premier Value Maximum Strength
- Generic name
- DEXTROMETHORPHAN HBR, GUAIFENESIN
- Manufacturer
- PHARMACY VALUE ALLIANCE LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 46bf124a-a44f-4066-b936-852d46da8f40
- SPL ID
- 54025a67-fd48-4ed1-a284-0a87e6755041
- Version
- 6
- Effective date
- 2024-10-28
- Source export date
- 2026-10-12
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:19:13
| 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 | M012 | openfda.application_number | |
| brand name | Premier Value Maximum Strength | openfda.brand_name | |
| generic name | DEXTROMETHORPHAN HBR, GUAIFENESIN | openfda.generic_name | |
| manufacturer name | PHARMACY VALUE ALLIANCE LLC | openfda.manufacturer_name | |
| ndc | package | 68016-740-04 | openfda.package_ndc |
| ndc | product | 68016-740 | openfda.product_ndc |
| ndc11 | package | 68016074004 | derived:openfda.package_ndc |
| rxcui | 1020138 | openfda.rxcui | |
| spl id | 54025a67-fd48-4ed1-a284-0a87e6755041 | id | |
| spl set id | 46bf124a-a44f-4066-b936-852d46da8f40 | set_id | |
| unii | 9D2RTI9KYH | openfda.unii | |
| unii | 495W7451VQ | 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.