87681-002 RAVYNDRA MAGNESIUM CREAM

Manufacturer
Guangzhou Xinhongda Trading Service Co., Ltd.
Effective date
2026-06-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-06-06 05:10:10

Label at a glance#

ProductRAVYNDRA Magnesium Cream
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

MENTHOL 10%
CAMPHOR 4%

OTC - PURPOSE SECTION

Topical analgesic

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 extemal use only.

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

When using this product, 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

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
EUCALYPTUS GLOBULUS LEAF OIL
DISODIUM EDTA
BOSWELLIA CARTERI OIL
CENTELLA ASIATICA EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
77dc03a4-fbfc-e6a3-fe95-285bbae40d75Product name220250814
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

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
87681-00287681-002-01

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-06-01daily-update2026-06-04 05:10:16

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
536950a2-112b-5266-e063-6394a90a678f532e2f62-0fb1-05b1-e063-6394a90ae5382026-06-04WarningsExact identifier
spl id: 536950a2-112b-5266-e063-6394a90a678f
spl set id: 532e2f62-0fb1-05b1-e063-6394a90ae538

Reported adverse events (FAERS/openFDA)#

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