Goldie's Pain Off Cream

Manufacturer
Goldie's Biohealth, LLC
Effective date
2018-02-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:03:18

Label at a glance#

ProductGoldies Pain Off
Active ingredientCAMPHOR (SYNTHETIC)
Label structure7 sections

Dosage and administration

Adults and children two-years of age or older: Apply to affected area not more than three to four daily. Children under two-years of age: consult a physician.

Label contents#

Full prescribing information#

Active ingredient:

OTC - ACTIVE INGREDIENT SECTION

Camphor 5.00%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS:

INDICATIONS & USAGE SECTION

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

WARNINGS:

WARNINGS SECTION

  • For external use only. 

Do not apply 

OTC - DO NOT USE SECTION

  • to wounds or damaged skin.
  • Avoid contact with eyes. If symptoms persist for more than seven days, discontinue use and consult physician.
  • Do not bandage tighty.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, consult physician.

If pregant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

contact physician before use.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

  • Adults and children two-years of age or older: Apply to affected area not more than three to four daily.
  • Children under two-years of age: consult a physician.

Additional information:

SPL UNCLASSIFIED SECTION

Store at room temperature.

Other Ingredients:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera Gel) Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Aqua (Deionized Water), Arnica Montana flower Extract, Boswellia Serrata Extract, Butyrospermum Parkii (Shea) Butter, Cetyl Esters, Cetyl Myristoleate, Citrus Aurantium Dulcis (Orange) Oil, Dimethicone, DMDM Hydantion, Emu Oil, Ethoxydiglycol, Ethylexylglycerin, Ethylhexyl Palmitate, Eucalyptus Globulus Oil, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Oil, Mentha Piperita (Peppermint) Oil, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Pyridoxine HC1 (Vitamin B6), Steareth-21, Tocopherol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71317-81571317-815-02, 71317-815-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 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
07241531-c609-b500-e063-6394a90aed7a4a9d2992-071c-0f20-e054-00144ff88e882023-10-07WarningsExact identifier
spl set id: 4a9d2992-071c-0f20-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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