Gold Bond

Manufacturer: Chattem, Inc.
Effective date: 2023-10-30
Label type: HUMAN OTC DRUG LABEL
Version: 14
Source: legacy-cache
Hydrated at: 2026-08-01 21:23:00

Label at a glance#

ProductGold Bond Original Strength

Active ingredientMENTHOL

Label structure15 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

a dults and children 2 years and older: apply freely up to 3 or 4 times daily c hildren 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

talc, zinc oxide, acacia senegal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate (309-004)

Gold Bond Medicated Extra Strength Body Powder

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.8%

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

talc, zinc oxide, acacia senegal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate (309-006)

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gold Bond
Medicated Healing Since 1908

Original Strength

BODY POWDER
Triple Action Relief
Cooling ● Absorbing ● Itch Relieving

Menthol 0.15%
Net wt 4 oz (113 g)

Gold Bond Medicated Healing Since 1908 Original Strength BODY POWDER Triple Action Relief Cooling ● Absorbing ● Itch Relieving Menthol 0.15% Net wt 4 oz (113 g)

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gold Bond
Healing Medicated Since 1908
Extra Strength

BODY POWDER

Triple Action Relief
Cooling ● Absorbing ● Itch Relieving

Menthol 0.8%
Net wt 4 oz (113 g)

Gold Bond Healing Medicated Since 1908 Extra Strength BODY POWDER Triple Action Relief Cooling ● Absorbing ● Itch Relieving Menthol 0.8% Net wt 4 oz (113 g)

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
41167-0404-0	GM - Gram	41167-0404	54f0a5f3-75aa-4252-80bc-7b7eef42e671	1	2018-03-08

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
MENTHOL	ACTIVE INGREDIENT	L7T10EIP3A	5
ZINC OXIDE	ACTIVE INGREDIENT	SOI2LOH54Z	5
MENTHOL	ACTIVE MOIETY	L7T10EIP3A	5
ZINC OXIDE	ACTIVE MOIETY	SOI2LOH54Z	5
ACACIA	INACTIVE INGREDIENT	5C5403N26O	5
EUCALYPTOL	INACTIVE INGREDIENT	RV6J6604TK	5
METHYL SALICYLATE	INACTIVE INGREDIENT	LAV5U5022Y	5
SALICYLIC ACID	INACTIVE INGREDIENT	O414PZ4LPZ	5
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	5
THYMOL	INACTIVE INGREDIENT	3J50XA376E	5
ZINC STEARATE	INACTIVE INGREDIENT	H92E6QA4FV	5

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Gold Bond Original Strength
Menthol
TALC
ZINC OXIDE
ACACIA
EUCALYPTOL
METHYL SALICYLATE
SALICYLIC ACID
THYMOL
ZINC STEARATE
Gold Bond Extra Strength

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
41167-0104	41167-0104-1, 41167-0104-0, 41167-0104-3, 41167-0104-6, 41167-0104-2
41167-0404	41167-0404-0, 41167-0404-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MENTHOL	L7T10EIP3A	ACTIB
TALC	7SEV7J4R1U	IACT
ZINC OXIDE	SOI2LOH54Z	IACT
ACACIA	5C5403N26O	IACT
EUCALYPTOL	RV6J6604TK	IACT
METHYL SALICYLATE	LAV5U5022Y	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
THYMOL	3J50XA376E	IACT
ZINC STEARATE	H92E6QA4FV	IACT
MENTHOL	L7T10EIP3A	ACTIB
TALC	7SEV7J4R1U	IACT
ZINC OXIDE	SOI2LOH54Z	IACT
ACACIA	5C5403N26O	IACT
EUCALYPTOL	RV6J6604TK	IACT
METHYL SALICYLATE	LAV5U5022Y	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
THYMOL	3J50XA376E	IACT
ZINC STEARATE	H92E6QA4FV	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 83 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
TALC	TALC	7SEV7J4R1U	POWDER, FOR SUSPENSION / ORAL		735 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, FILM COATED / ORAL		91 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	POWDER, FOR SOLUTION / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	TABLET, EXTENDED RELEASE / ORAL	36 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	CAPSULE, DELAYED RELEASE / ORAL		420 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
EUCALYPTOL	EUCALYPTOL	RV6J6604TK	PASTE, DENTIFRICE / DENTAL	2.4 %w/w		Exact identifier — unii candidate 7 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	SUSPENSION / ORAL		234 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	DOUCHE / VAGINAL	0.05 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	POWDER / TOPICAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	LOZENGE / ORAL		50 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET / ORAL	70 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, EXTENDED RELEASE / ORAL		300 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, ORALLY DISINTEGRATING / ORAL		80 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, FOR SUSPENSION / ORAL		24 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	LOZENGE / ORAL		53 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	TABLET, COATED / ORAL	1.82 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	CAPSULE / ORAL	2.04 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET / RECTAL	32.4 mg		Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, SUGAR COATED / ORAL	NA		Exact identifier — unii candidate 35 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	OINTMENT / TOPICAL	NA		Exact identifier — unii candidate 12 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	PELLET / ORAL		69 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET, EXTENDED RELEASE / ORAL	34.4 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET / SUBLINGUAL	9.1 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	CAPSULE, COATED / ORAL		87 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
THYMOL	THYMOL	3J50XA376E	LIQUID / RESPIRATORY (INHALATION)	0.01 %w/w		Exact identifier — unii candidate 2 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET / BUCCAL	9.1 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	SUSPENSION / INTRAMUSCULAR	1 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
EUCALYPTOL	EUCALYPTOL	RV6J6604TK	JELLY / NASAL	68.5 mg		Exact identifier — unii candidate 7 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET, ORALLY DISINTEGRATING / ORAL		7 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, CHEWABLE, EXTENDED RELEASE / ORAL		18 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	GRANULE, FOR SUSPENSION / ORAL		296 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	GEL / TOPICAL	0.05 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	GRANULE, DELAYED RELEASE / ORAL		525 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	CAPSULE, COATED PELLETS / ORAL	14 mg		Exact identifier — unii candidate 35 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	TABLET / ORAL	10 mg		Exact identifier — unii candidate 8 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	OINTMENT / TOPICAL	74.6 %w/w		Exact identifier — unii candidate 35 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET, COATED / ORAL	156 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET / ORAL	1000 mg		Exact identifier — unii candidate 35 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	TABLET / SUBLINGUAL	2.5 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	POWDER / TOPICAL		9235 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	TABLET / BUCCAL	2.5 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	CAPSULE / ORAL		20 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	CREAM / TOPICAL	6 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	POWDER / ORAL	800 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	SHAMPOO / TOPICAL	2 %w/w		Exact identifier — unii candidate 12 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	SUSPENSION / ORAL		2 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	TABLET, DELAYED RELEASE / ORAL		349 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
EUCALYPTOL	EUCALYPTOL	RV6J6604TK	CAPSULE / ORAL	NA		Exact identifier — unii candidate 7 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	SYRUP / ORAL	NA		Exact identifier — unii candidate 12 equally ranked IID candidates
EUCALYPTOL	EUCALYPTOL	RV6J6604TK	DROPS / NASAL	0.2 mg/1ml		Exact identifier — unii candidate 7 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	TABLET, FILM COATED / ORAL	15.2 mg		Exact identifier — unii candidate 12 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	GUM, CHEWING / BUCCAL		280 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
EUCALYPTOL	EUCALYPTOL	RV6J6604TK	DROPS / OPHTHALMIC	0.02 %w/w		Exact identifier — unii candidate 7 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	TABLET, DELAYED RELEASE / ORAL	30 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	GRANULE / ORAL		322 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	SUSPENSION, EXTENDED RELEASE / ORAL		46 mg	Exact identifier — unii candidate 35 equally ranked IID candidates
TALC	TALC	7SEV7J4R1U	ELIXIR / ORAL	4.5 mg/5ml		Exact identifier — unii candidate 35 equally ranked IID candidates
ZINC STEARATE	ZINC STEARATE	H92E6QA4FV	TABLET / ORAL		72 mg	Exact identifier — unii candidate 12 equally ranked IID candidates
ACACIA	ACACIA	5C5403N26O	CAPSULE, EXTENDED RELEASE / ORAL		64 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
METHYL SALICYLATE	METHYL SALICYLATE	LAV5U5022Y	POWDER, DENTIFRICE / DENTAL	NA		Exact identifier — unii candidate 8 equally ranked IID candidates

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
9a3f2598-3385-4956-b0f4-86b2306b6cd8			dd74205d-4520-417e-b43f-6622c35c1971	2023-12-07	Warnings	Exact identifier spl set id: dd74205d-4520-417e-b43f-6622c35c1971

Reported adverse events (FAERS/openFDA)#

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