Gold Bond Medicated Original Strength Body

Manufacturer: Chattem, Inc.
Effective date: 2025-01-08
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 00:51:14

Label at a glance#

ProductGold Bond Medicated Original Strength Body

Active ingredientMENTHOL

Label structure9 sections

Indications and uses

temporarily relieves the pain and itch associated with: ■ minor cuts ■ sunburn ■ insect bites ■ scrapes ■ minor burns ■ minor skin irritations

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 ■ for best results dry skin thoroughly before applying

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Gold Bond Medicated

Original Strength Body Powder

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15%

Purpose

OTC - PURPOSE SECTION

Anti-itch

Uses

INDICATIONS & USAGE SECTION

temporarily relieves the pain and itch associated with:

■ minor cuts ■ sunburn ■ insect bites ■ scrapes ■ minor burns ■ minor skin irritations

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

■ for best results dry skin thoroughly before applying

Inactive ingredients

INACTIVE INGREDIENT SECTION

zea mays (corn) starch, zinc oxide, acacia senegal gum, silica, tricalcium phosphate, eucalyptol, methyl salicylate, salicylic acid, zinc stearate, thymol

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOLD BOND
ORIGINAL STRENGTH
BODY POWDER
Net wt 10 oz (283 g)
GOLD BOND ORIGINAL STRENGTH BODY POWDER Net wt 10 oz (283 g)

PRINCIPAL DISPLAY PANEL GOLD BOND ORIGINAL STRENGTH BODY POWDER Net wt 10 oz (283 g)

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

GOLD BOND
MEDICATED
ORIGINAL STRENGTH
BODY POWDER
Net wt 1 OZ (28 g)

GOLD BOND MEDICATED ORIGINAL STRENGTH BODY POWDER Net wt 1 OZ (28 g)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1431703	menthol 0.15 % Topical Powder	PSN	5
1431703	menthol 0.0015 MG/MG Topical Powder	SCD	5
1431703	menthol 0.15 % Topical Powder	SY	5
1431703	menthol 1.5 MG per GM Topical Powder	SY	5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
41167-0110-0	Gold Bond Medicated Original Strength Body	28 g in 1 BOTTLE	POWDER	28	5
41167-0110-6	Gold Bond Medicated Original Strength Body	113 g in 1 BOTTLE	POWDER	113	5
41167-0110-9	Gold Bond Medicated Original Strength Body	283 g in 1 BOTTLE	POWDER	283	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
41167-0110	GOLD BOND MEDICATED ORIGINAL STRENGTH BODY (MENTHOL) POWDER [CHATTEM, INC.]	5	Legacy NDC, 3 package rows	20250109_e346fdda-d9b0-4277-9acb-7f56ea0db056.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
41167-0110-6	GM - Gram	41167-0110	965480c9-7786-457c-83d6-d6e519298ae8	1	2022-06-06
41167-0110-9	GM - Gram	41167-0110	3771fe56-6fa2-4ced-814d-01be2c55090b	1	2022-06-06

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Gold Bond Medicated Original Strength Body
Menthol
STARCH, CORN
ZINC OXIDE
ACACIA
SILICON DIOXIDE
TRICALCIUM PHOSPHATE
EUCALYPTOL
METHYL SALICYLATE
SALICYLIC ACID
ZINC STEARATE
THYMOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41167-0110	41167-0110-9, 41167-0110-6, 41167-0110-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
STARCH, CORN	O8232NY3SJ	IACT
ZINC OXIDE	SOI2LOH54Z	IACT
ACACIA	5C5403N26O	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
TRICALCIUM PHOSPHATE	K4C08XP666	IACT
EUCALYPTOL	RV6J6604TK	IACT
METHYL SALICYLATE	LAV5U5022Y	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
ZINC STEARATE	H92E6QA4FV	IACT
THYMOL	3J50XA376E	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
2a265301-c8de-43f3-829d-841c408c3799			e346fdda-d9b0-4277-9acb-7f56ea0db056	2025-01-08	Warnings	Exact identifier spl id: 2a265301-c8de-43f3-829d-841c408c3799 spl set id: e346fdda-d9b0-4277-9acb-7f56ea0db056

Reported adverse events (FAERS/openFDA)#

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