Natural Pain Relief Foot Cream

Manufacturer
Neat Feat Products Limited
Effective date
2025-01-08
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:30:09

Label at a glance#

ProductNatural Pain Relief Foot Cream
Active ingredientCAMPHOR (NATURAL)
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 g NDC: 50017-033-01 Label 50 gLabel 50 g

OTC - ACTIVE INGREDIENT SECTION

Camphor 3% .................... Natural Pain Relieving Cream

OTC - PURPOSE SECTION

For the temporary relief of pain

WARNINGS SECTION

For external use only.

Avoid con1act with eyes.

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

Do not use on broken or irritated skin.

Slop use and ask a doctor if skin irritation develops.

If pregnant or tnnt feeding, ask a health professional before use.

Keep out of reach of chlklren, in case of overdose, get medical help or contact a poison control center right away.

INDICATIONS & USAGE SECTION

For the temporary relief of pain.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childen, in case of overdose, get medical help or contact a poison control center right away.

DOSAGE & ADMINISTRATION SECTION


Adults and chlldren 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 doclor.

OTHER SAFETY INFORMATION

Shake well prior to use.

Store below 30C/86F

INACTIVE INGREDIENT SECTION

Decyl Polyglucoside, Water, Sorbitan Oleate, Glycerin, Peppermint Oil, Rosemary Oil, Frankincense Oil, Amica Montana Extract, Cajeput Oil, Eucalyptus Oil, Clove Bud Oil, Potassium Sorbate, Anhydrous Citric Acid.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50017-033NATURAL PAIN RELIEF FOOT CREAM (CAMPHOR) CREAM [NEAT FEAT PRODUCTS LIMITED]7Legacy NDC20250110_897dcd0c-ee8c-1709-e053-2a95a90ad2c2.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50017-03350017-033-01, 50017-033-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
41ea3893-2269-d0dd-e063-6394a90ae86f897dcd0c-ee8c-1709-e053-2a95a90ad2c22025-10-24WarningsExact identifier
spl set id: 897dcd0c-ee8c-1709-e053-2a95a90ad2c2

Reported adverse events (FAERS/openFDA)#

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