Home FDA labels 462e6f04-7a66-e4fe-e063-6394a90af0f9 LEG CRAMPS PM 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 (canonical bytes are SHA-256 checked before publication)
Brand name LEG CRAMPS PM
Generic name OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFUR
Manufacturer Walgreen Company
Product type HUMAN OTC DRUG
SPL set ID d8c7ec58-5453-0e58-e053-2995a90abff1
SPL ID 462e6f04-7a66-e4fe-e063-6394a90af0f9
Version 3
Effective date 2025-12-17
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 table 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.
Harmonized identifiers page 1 of 1 · 18 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name LEG CRAMPS PM openfda.brand_name generic name OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFUR openfda.generic_name manufacturer name Walgreen Company openfda.manufacturer_name ndc package 0363-7174-14 openfda.package_ndc ndc product 0363-7174 openfda.product_ndc ndc11 package 00363717414 derived:openfda.package_ndc spl id 462e6f04-7a66-e4fe-e063-6394a90af0f9 id spl set id d8c7ec58-5453-0e58-e053-2995a90abff1 set_id unii 789U1901C5 openfda.unii unii DD5FO1WKFU openfda.unii unii HF539G9L3Q openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 2E32821G6I openfda.unii unii 6IO182RP7A openfda.unii unii S003A158SB openfda.unii unii 70FD1KFU70 openfda.unii unii G0R4UBI2ZZ openfda.unii unii C88X29Y479 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Warnings A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur. • If pregnant or breast-feeding, ask a health professional before use. Stop use and ask a doctor if: • You experience new or worsening symptoms. • Symptoms last longer than 3 days. • Keep out of reach of children. • In case of overdose, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.