Golden Remedy Pain Relief Balm

Manufacturer
GOLDEN CARE BOTANICALS LLC
Effective date
2025-08-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:40

Label at a glance#

ProductGolden Remedy Pain Relief Balm
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure9 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Topical analgesic for temporary relief of minor aches and pain of muscles and joints associated with backach, arthritis, strains, brusies, and sprains

OTC - DO NOT USE SECTION

Do not use on open wounds, broken skin, or with a heating pad

OTC - STOP USE SECTION

Stop use and ask a doctor if: condition worsens, or symptoms persist for more than 7 days.

WARNINGS SECTION

For external use only

INACTIVE INGREDIENT SECTION

Inactive ingredients: beeswax, avocado oil, shea butter, cocoa butter, mango butter, menthol crystals, avocado seed powder, camphor, helichrysum, frankincense, ginger oil, vitamin e

DOSAGE & ADMINISTRATION SECTION

Directions:
Adults and children 12 years and over: Apply to the affected area not more than 3 to 4 times daily.

Route of Administration:Topical (external) use only

INDICATIONS & USAGE SECTION

Route of Administration:Topical

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek immediate medical attention or contact Poison Control

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85g NDC 87937-001-0285g NDC 87937-001-0257g NDC 87937-001-0157g NDC 87937-001-01

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87037-00187037-001-01, 87037-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

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
4ff8c0e4-8cea-7be1-e063-6394a90aacaa3c6b0114-0bc9-a150-e063-6394a90a191d2026-04-21WarningsExact identifier
spl set id: 3c6b0114-0bc9-a150-e063-6394a90a191d

Reported adverse events (FAERS/openFDA)#

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