warnings
Warnings: If symptoms persist or worsen or if pregnant or nursing consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.
Hangover 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
- Hangover Relief
- Generic name
- ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC.
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 93b4a184-572c-48ef-9fc0-8e357a1e0d1b
- SPL ID
- 7d538d9b-6a91-ffe3-e053-2a91aa0a8f47
- Version
- 2
- Effective date
- 2018-12-18
- 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 20:07:26
| Harmonized routes |
|---|
| SUBLINGUAL |
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 |
|---|---|---|---|
| brand name | Hangover Relief | openfda.brand_name | |
| generic name | ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC. | openfda.generic_name | |
| manufacturer name | Homeocare Laboratories | openfda.manufacturer_name | |
| ndc | package | 61727-330-21 | openfda.package_ndc |
| ndc | product | 61727-330 | openfda.product_ndc |
| ndc11 | package | 61727033021 | derived:openfda.package_ndc |
| spl id | 7d538d9b-6a91-ffe3-e053-2a91aa0a8f47 | id | |
| spl set id | 93b4a184-572c-48ef-9fc0-8e357a1e0d1b | set_id | |
| unii | 00UK7646FG | openfda.unii | |
| unii | PQM9SA369U | openfda.unii | |
| unii | 269XH13919 | openfda.unii | |
| unii | W9FZA51AS1 | openfda.unii | |
| unii | O40UQP6WCF | openfda.unii | |
| unii | AEQ8NXJ0MB | openfda.unii | |
| unii | VSW71SS07I | openfda.unii | |
| unii | T4423S18FM | openfda.unii | |
| unii | J41CSQ7QDS | 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.