Golden Remedy Extra Strength

Manufacturer
Golden Care Botanicals LLC
Effective date
2025-09-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:20

Label at a glance#

ProductGolden Remedy Extra Strength
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol 4.3%................External analgesic

Camphor 4.3%..............External analgesic

OTC - PURPOSE SECTION

Topical analgesic for temporary relief of pain/itching due to sunburn, minor burns, insect bites, and everyday aches

OTC - DO NOT USE SECTION

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

WARNINGS SECTION

For external use only

OTC - STOP USE SECTION

Stop use and ask a medical doctor if condition worsens, or symptoms persist

INACTIVE INGREDIENT SECTION

Inactive ingredients: Aaloe vera juice, Witch hazel, Avocado oil, Menthol crystals, Camphor, Ginger essential oil, Frankincense essential oil, Helichrysum essential oil, Optiphen, and Vitamin E

DOSAGE & ADMINISTRATION SECTION

Directions: Adults and children 12+ years and older. Apply to affected area not more than 3-4 times per day

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

57g NDC 87037-00257g NDC 87037-002

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87037-00287037-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
4ff89acb-6640-0cc2-e063-6394a90aba8e3fbbe613-6a5b-5fd1-e063-6394a90a74222026-04-21WarningsExact identifier
spl set id: 3fbbe613-6a5b-5fd1-e063-6394a90a7422

Reported adverse events (FAERS/openFDA)#

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