Gold Bond Medicated Maximum Strength Foot

Manufacturer: Chattem, Inc.
Effective date: 2025-07-22
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:07:55

Label at a glance#

ProductGold Bond Medicated Maximum Strength Foot

Active ingredientMENTHOL

Label structure8 sections

Indications and uses

temporarily relieves the pain and itch associated with: ■ minor skin irritations on the foot

Dosage and administration

■ adults and children 2 years and older: apply freely up to 3 or 4 times daily ■ children under 2 years: ask a doctor ■ thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. Sprinkle inside shoes for maximum freshness.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Gold Bond Medicated

Foot Powder

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 1%

Purpose

OTC - PURPOSE SECTION

Anti-itch

Uses

INDICATIONS & USAGE SECTION

temporarily relieves the pain and itch associated with:

■ minor skin irritations on the foot

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

■ avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ condition worsens

■ symptoms persist for more than 7 days or clear up and occur again within a few days

■ redness, irritation, swelling or pain persists or increases

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ adults and children 2 years and older: apply freely up to 3 or 4 times daily

■ children under 2 years: ask a doctor

■ thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. Sprinkle inside shoes for maximum freshness.

Inactive ingredients

INACTIVE INGREDIENT SECTION

zea mays (corn) starch, sodium bicarbonate, acacia senegal gum, silica, tricalcium phosphate, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil, benzethonium chloride

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOLD BOND
MEDICATED
MAXIMUM STRENGTH
FOOT POWDER
ANTI-ITCH MENTHOL 1%
TRIPLE ACTION FORMULA
Net Wt 10 oz (283 g)

GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT POWDER ANTI-ITCH MENTHOL 1% TRIPLE ACTION FORMULA Net Wt 10 oz (283 g)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
259579	menthol 1 % Topical Powder	PSN	4
259579	menthol 0.01 MG/MG Topical Powder	SCD	4
259579	menthol 1 % Topical Powder	SY	4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
41167-0171-2	Gold Bond Medicated Maximum Strength Foot	283 g in 1 BOTTLE	POWDER	283		4
41167-0171-6	Gold Bond Medicated Maximum Strength Foot	113 g in 1 BOTTLE	POWDER	113		4

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
41167-0171-6	GM - Gram	41167-0171	921cd005-9f4a-4424-bd9c-7f758adc5562	1	2022-06-06

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

Gold Bond Medicated Maximum Strength Foot
Menthol
STARCH, CORN
SODIUM BICARBONATE
ACACIA
SILICON DIOXIDE
TRICALCIUM PHOSPHATE
EUCALYPTUS OIL
PEPPERMINT OIL
BENZETHONIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41167-0171	41167-0171-2, 41167-0171-6

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
STARCH, CORN	O8232NY3SJ	IACT
SODIUM BICARBONATE	8MDF5V39QO	IACT
ACACIA	5C5403N26O	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
TRICALCIUM PHOSPHATE	K4C08XP666	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
BENZETHONIUM CHLORIDE	PH41D05744	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f5d4a110-c724-4878-8df3-be80292a8390			bb9cbd03-3254-4411-9b4f-e81908a41bd1	2025-07-22	Warnings	Exact identifier spl id: f5d4a110-c724-4878-8df3-be80292a8390 spl set id: bb9cbd03-3254-4411-9b4f-e81908a41bd1