FDA.reportPublic FDA data

87681-011 LQNZJBAU Magnesium Cream

Manufacturer
Guangzhou Xinhongda Trading Service Co., Ltd.
Effective date
2026-06-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
weekly-update
Hydrated at
2026-07-17 21:41:39

Label at a glance#

ProductLQNZJBAU Magnesium Cream
Active ingredientMAGNESIUM SULFATE HEPTAHYDRATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Magnesium Sulfate Heptahydrate 1X HPUS

OTC - PURPOSE SECTION

Muscle soothing

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with :
simple backache, arthritis, strains, bruises, and sprains.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not apply to wounds or damaged skin.
Do not bandage tightly.

OTC - WHEN USING SECTION

Avoid contact with eyes.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7
days or clear up and occur again within a few days.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control
Center right away.

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

INACTIVE INGREDIENT SECTION

WATER
PROPYLENE GLYCOL
CETEARYL ALCOHOL
GLYCERIN
ALOE BARBADENSIS LEAF JUICE
ISOPROPYL MYRISTATE
MAGNESIUM CHLORIDE
NIACINAMIDE
GLYCERYL STEARATE
CAPRYLIC/CAPRIC TRIGLYCERIDE
PEG-100 STEARATE
CETYL ALCOHOL
HYDROXYETHYLCELLULOSE
PHENOXYETHANOL
DIMETHICONE
TOCOPHERYL ACETATE
ETHYLHEXYLGLYCERIN
TROMETHAMINE
XANTHAN GUM
ARNICA MONTANA
EUCALYPTUS GLOBULUS LEAF OIL
DISODIUM EDTA
BOSWELLIA CARTERI OIL
CENTELLA ASIATICA EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87681-01187681-011-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CETYL ALCOHOL936JST6JCNIACT
FRANKINCENSE OIL67ZYA5T02KIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
NIACINAMIDE25X51I8RD4IACT
GLYCERYL STEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
HYDROXYETHYLCELLULOSET4V6TWG28DIACT
DIMETHICONE92RU3N3Y1OIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
CETEARYL ALCOHOL2DMT128M1SIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EUCALYPTUS GLOBULUS LEAF OIL2R04ONI662IACT
XANTHAN GUMTTV12P4NEEIACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
TROMETHAMINE023C2WHX2VIACT
ARNICA MONTANAO80TY208ZWIACT
WATER059QF0KO0RIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
EDETATE DISODIUM7FLD91C86KIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5570b5f1-0de6-5008-e063-6294a90ae7255570b5f1-0de5-5008-e063-6294a90ae7252026-06-29WarningsExact identifier
spl id: 5570b5f1-0de6-5008-e063-6294a90ae725
spl set id: 5570b5f1-0de5-5008-e063-6294a90ae725

Reported adverse events (FAERS/openFDA)#

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