warnings
Warnings Ask a doctor before use if you are sensitive to quinine. If pregnant or breastfeeding ask a health professional before use. Stop use and ask a doctor if symptoms persist for more than 7 days or worsen. Keep out of reach of children
LEG CRAMPS
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
- LEG CRAMPS
- Generic name
- CINCHONA OFFICINALIS BARK, ACONITUM NAPELLUS, PSEUDOGNAPHALIUM OBTUSIFOLIUM, LEDUM PALUSTRE TWIG, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, AND VISCUM ALBUM FRUITING TOP
- Manufacturer
- Hyland's Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 77630c9b-880d-4de1-ae25-5a01050727f7
- SPL ID
- ec71c58d-a5f0-d6a5-e053-2995a90a2ab2
- Version
- 12
- Effective date
- 2022-11-02
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:32
| 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 |
|---|---|---|---|
| brand name | LEG CRAMPS | openfda.brand_name | |
| generic name | CINCHONA OFFICINALIS BARK, ACONITUM NAPELLUS, PSEUDOGNAPHALIUM OBTUSIFOLIUM, LEDUM PALUSTRE TWIG, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, AND VISCUM ALBUM FRUITING TOP | openfda.generic_name | |
| manufacturer name | Hyland's Inc. | openfda.manufacturer_name | |
| ndc | package | 54973-3114-1 | openfda.package_ndc |
| ndc | package | 54973-3114-3 | openfda.package_ndc |
| ndc | package | 54973-3114-5 | openfda.package_ndc |
| ndc | package | 54973-3114-4 | openfda.package_ndc |
| ndc | package | 54973-3114-2 | openfda.package_ndc |
| ndc | package | 54973-3114-7 | openfda.package_ndc |
| ndc | product | 54973-3114 | openfda.product_ndc |
| ndc11 | package | 54973311403 | derived:openfda.package_ndc |
| ndc11 | package | 54973311407 | derived:openfda.package_ndc |
| ndc11 | package | 54973311404 | derived:openfda.package_ndc |
| ndc11 | package | 54973311405 | derived:openfda.package_ndc |
| ndc11 | package | 54973311402 | derived:openfda.package_ndc |
| ndc11 | package | 54973311401 | derived:openfda.package_ndc |
| spl id | ec71c58d-a5f0-d6a5-e053-2995a90a2ab2 | id | |
| spl set id | 77630c9b-880d-4de1-ae25-5a01050727f7 | set_id | |
| unii | 877L01IZ0P | openfda.unii | |
| unii | HF539G9L3Q | openfda.unii | |
| unii | 6IO182RP7A | openfda.unii | |
| unii | S003A158SB | openfda.unii | |
| unii | 36XQ854NWW | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | BK9092J5MP | 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.