Gold Bond Medicated Extra Strength Body

Manufacturer
Gold Bond Co LLC
Effective date
2025-12-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:19:55

Label at a glance#

ProductGold Bond Medicated Extra Strength Body
Active ingredientMENTHOL
Label structure8 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

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

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

GOLDBOND
EXTRA STRENGTH
BODY POWDER
Net wt 10 oz (283 g)

GOLDBOND EXTRA STRENGTH BODY POWDER Net wt 10 oz (283 g)GOLDBOND EXTRA STRENGTH BODY POWDER Net wt 10 oz (283 g)

PRINCIPAL DISPLAY PANEL GOLDBOND EXTRA STRENGTH BODY POWDER Net wt 10 oz (283 g)PRINCIPAL DISPLAY PANEL GOLDBOND EXTRA STRENGTH BODY POWDER Net wt 10 oz (283 g)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2169968menthol 0.8 % Topical PowderPSN1
2169968menthol 0.008 MG/MG Topical PowderSCD1
2169968menthol 8 MG per GM Topical PowderSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData Matrix0166534-01gold-bond-medicated-extra-strength-body-powder-02.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84714-0410-4Gold Bond Medicated Extra Strength Body283 g in 1 BOTTLEPOWDER2831
84714-0410-5Gold Bond Medicated Extra Strength Body113 g in 1 BOTTLEPOWDER1131

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84714-041084714-0410-5, 84714-0410-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
Gold Bond Medicated Extra Strength BodyMENTHOLGold Bond Co LLC7b75b7de-9c0b-4edf-b923-320f7d2bb1e62025-12-04WarningsExact identifier
ndc (package): 84714-0410-5
ndc (package): 84714-0410-4
ndc (product): 84714-0410
ndc11 (package): 84714041005
ndc11 (package): 84714041004
spl id: d60e260e-f7fe-4c69-a6ab-232b59540a47
spl set id: 7b75b7de-9c0b-4edf-b923-320f7d2bb1e6

Reported adverse events (FAERS/openFDA)#

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