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: Hyland's Inc.
Product type: HUMAN OTC DRUG
SPL set ID: b0574a7e-88fa-417e-b6d5-60ced59eba47
SPL ID: 56b343d8-714f-f4d4-e063-6394a90a81c5
Version: 18
Effective date: 2026-07-15
Source export date: 2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:29:59

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 · 26 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		Hyland's Inc.	openfda.manufacturer_name
ndc	package	54973-3093-7	openfda.package_ndc
ndc	package	54973-3093-8	openfda.package_ndc
ndc	package	54973-3093-2	openfda.package_ndc
ndc	package	54973-3093-1	openfda.package_ndc
ndc	package	54973-3093-6	openfda.package_ndc
ndc	product	54973-3093	openfda.product_ndc
ndc11	package	54973309306	derived:openfda.package_ndc
ndc11	package	54973309302	derived:openfda.package_ndc
ndc11	package	54973309308	derived:openfda.package_ndc
ndc11	package	54973309307	derived:openfda.package_ndc
ndc11	package	54973309301	derived:openfda.package_ndc
spl id		56b343d8-714f-f4d4-e063-6394a90a81c5	id
spl set id		b0574a7e-88fa-417e-b6d5-60ced59eba47	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 Ask a doctor before use if you are sensitive to quinine. Stop use and ask a doctor if symptoms persist for more than 7 days or worsen. If pregnant or breastfeeding Ask a health professional before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.