FDA.reportPublic FDA data

FOOT

Manufacturer
Smith Amish, LLC
Effective date
2025-12-12
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:22:38

Label at a glance#

ProductFOOT
Active ingredientMENTHOL
Label structure11 sections

Indications and uses

For temporary relief of minor aches and pains

Dosage and administration

Adults and children 2 years of age and over: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age consult a doctor.

Label contents#

Full prescribing information#

Drug Facts Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1.25%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains

Warnings

WARNINGS SECTION

  • For external use only
  • Avoid contact with eyes

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and over: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age consult a doctor.

Other information

OTHER SAFETY INFORMATION

Protect from excessive heat

Store at 20-25 oC (68-77F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Arnica montana flower extract, cetyl palmitate, ethylhexylglycerin, glycerin, glyceryl stearate, jojoba (Buxus chinensis) oil, peppermint (mentha piperita) oil, phenoxyethanol, sodium citrate, stearic acid, sweet almond (Prunus amydgalus dulcis) oil, tea tree (Melaleuca alternifolia) oil, tocopherol (Vitamin E), water

Questions?

OTC - QUESTIONS SECTION

Call (866) 419-3567

Monday through Friday 8:00am - 2:00pm ET

SPL UNCLASSIFIED SECTION

Tamper evident: Do not use if safety seal under cap is broken or missing.

Manufactured for Smith Amish LLC 16350 N Hwy 329 Reddick, FL 32634

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Smith Amish Arthritis Cream (72609-702-02)

Provides Penetrating Relief

  • Arthritic pain
  • Muscle Pain
  • Joint Pain
  • Back Pain

Fresh scent from Arnica & Eucalyptus

All natural and non-greasy

Net wt. 2oz (59g)

labellabel

Smith Amish Eczema Cream (4oz) - 72609-704-04

4oz foot cream4oz foot cream

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416982menthol 1.25 % Topical CreamPSN6
416982menthol 12.5 MG/ML Topical CreamSCD6
416982menthol 1.25 % Topical CreamSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130869372000274GTIN-13: 0869372000274
EAN-13: 0869372000274
GTIN-12: 869372000274
UPC-A: 869372000274
GTIN storage (14 digits): 00869372000274		foot cream4.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72609-703-022025-07-29C16284748780-13b156c62-2843-fb37-e063-e6dba90a4e07Smith Amish Foot Cream (2oz) - 72609-703-02; Smith Amish Foot Cream (4oz) - 72609-703-04

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72609-703-02FOOT59 g in 1 TUBECREAM596
72609-703-02FOOT1 in 1 BOXCREAM16
72609-703-04FOOT123 g in 1 JARCREAM1236

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
72609-70372609-703-02, 72609-703-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ETHYLHEXYLGLYCERIN147D247K3PIACT
ALMOND OIL66YXD4DKO9IACT
MENTHOLL7T10EIP3AACTIB
JOJOBA OIL724GKU717MIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEPPERMINT OILAV092KU4JHIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ARNICA MONTANA WHOLEO80TY208ZWIACT
CETYL PALMITATE5ZA2S6B08XIACT
SODIUM CITRATE1Q73Q2JULRIACT
STEARIC ACID4ELV7Z65APIACT
TEA TREE OILVIF565UC2GIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
FOOTMENTHOLSmith Amish, LLC20c48537-f55f-c10f-e063-6394a90a4cca2025-12-12WarningsExact identifier
ndc (package): 72609-703-02
ndc (package): 72609-703-04
ndc (product): 72609-703
ndc11 (package): 72609070304
ndc11 (package): 72609070302
spl id: 45c89ca7-3353-d315-e063-6394a90ac647
spl set id: 20c48537-f55f-c10f-e063-6394a90a4cca

Reported adverse events (FAERS/openFDA)#

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