FDA.reportPublic FDA data

Gold Bond Medicated Original Strength Body

Manufacturer
Navajo Manufacturing Company Inc.
Effective date
2024-10-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:22:40

Label at a glance#

ProductGold Bond Medicated Original Strength Body
Active ingredientMENTHOL
Label structure7 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 BondGold Bond

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1431703menthol 0.15 % Topical PowderPSN2
1431703menthol 0.0015 MG/MG Topical PowderSCD2
1431703menthol 0.15 % Topical PowderSY2
1431703menthol 1.5 MG per GM Topical PowderSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67751-225-01Gold Bond Medicated Original Strength Body28 g in 1 BOTTLEPOWDER282
67751-225-01Gold Bond Medicated Original Strength Body1 in 1 BLISTER PACKPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67751-225GOLD BOND MEDICATED ORIGINAL STRENGTH BODY (MENTHOL) POWDER [NAVAJO MANUFACTURING COMPANY INC.]2Current NDC, 2 package rows20241004_f71d598c-92c3-d6fd-e053-6394a90a97d7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
41167-0110-6GM - Gram41167-0110965480c9-7786-457c-83d6-d6e519298ae812022-06-06
41167-0110-9GM - Gram41167-01103771fe56-6fa2-4ced-814d-01be2c55090b12022-06-06

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
67751-22567751-225-01
41167-0110

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
NameUNIIKind
STARCH, CORNO8232NY3SJIACT
ZINC OXIDESOI2LOH54ZIACT
ACACIA5C5403N26OIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
EUCALYPTOLRV6J6604TKIACT
METHYL SALICYLATELAV5U5022YIACT
SALICYLIC ACIDO414PZ4LPZIACT
ZINC STEARATEH92E6QA4FVIACT
THYMOL3J50XA376EIACT
MENTHOLL7T10EIP3AACTIB

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 Original Strength BodyMENTHOLNavajo Manufacturing Company Inc.f71d598c-92c3-d6fd-e053-6394a90a97d72024-10-03WarningsExact identifier
ndc (package): 67751-225-01
ndc (product): 67751-225
ndc11 (package): 67751022501
spl id: 23966402-d6b2-fd89-e063-6394a90ab886
spl set id: f71d598c-92c3-d6fd-e053-6394a90a97d7

Reported adverse events (FAERS/openFDA)#

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