FDA.reportPublic FDA data

Medicated Body

Manufacturer
Walmart Stores Inc
Effective date
2016-12-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:48:12

Label at a glance#

ProductMedicated Body Powder
Active ingredientMENTHOL, ZINC OXIDE
Label structure10 sections

Indications and uses

for the temporary relief of the pain and itch associated with minor cuts scrapes sunburn insect bites prickly heat rashes minor burns minor skin irritations dries the oozing of poison ivy, oak and sumac.

Dosage and administration

adults and children 2 years and older, apply freely up to 3 or 4 times daily under 2 years: ask a doctor before using for best results, dry skin thoroughly before use

Label contents#

Full prescribing information#

Drug FactsActive Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15 %

Zinc Oxide 1.0%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of the pain and itch associated with

  • minor cuts
  • scrapes
  • sunburn
  • insect bites
  • prickly heat
  • rashes
  • minor burns
  • minor skin irritations
  • dries the oozing of poison ivy, oak and sumac.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidential ingestion, get medical help or contact a Poison Control Center right away.

Warnings

WARNINGS SECTION

For external use only

When usin this product

OTC - WHEN USING SECTION

Avoid contact with eyes. Not for genital area.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms do not get better within 7 days or clear up and occur again within a few days

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older, apply freely up to 3 or 4 times daily
  • under 2 years: ask a doctor before using
  • for best results, dry skin thoroughly before use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Talc, Acacia, Eucalyputus Oil, Menthyl Salicylate, Salicylic Acid, Thymol, Zinc Stearate

equate Medicated Body Powder product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49035-295-10

equate™

Compare to GoldBond® Medicated Body Powder Active Ingredients

Medicated Body Powder

4 X Relief

  • Relieves Itcing
  • Cools Skin
  • Absorbs Moisture
  • Helps Protect skin

Menthol 0.15%

NET WT 10 OZ (283g)

Medicated Body Powder

Satisfaction guarenteed- or we'll replace it or give you your money back.

For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915

DISTRIBUTED BY:
Wal-Mart Stores, Inc.,

Bentonville, AR 72716

PRODUCT OF IINDIA

*This product is not manufactured or distributed by Chattem, Inc., owner of the registered trademark Gold Bond® Medicated body Powder.

DNH/C-92

PC WM Medi PowderPC WM Medi Powder

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
577232menthol 0.15 % / zinc oxide 1 % Topical PowderPSN1
577232menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical PowderSCD1
577232Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical PowderSY1
577232menthol 0.15 % / zinc oxide 1 % Topical PowderSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-295-10Medicated BodyPowder283 g in 1 BOTTLEPOWDER2831

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-295MEDICATED BODY POWDER (MENTHOL, ZINC OXIDE) POWDER [WALMART STORES INC]1Legacy NDC, 1 package rows20161219_206cd4f9-5829-41aa-8187-16728bcabfd7.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-29549035-295-10

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
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
ZINC OXIDESOI2LOH54ZACTIB
TALC7SEV7J4R1UIACT
ACACIA5C5403N26OIACT
EUCALYPTUS OIL2R04ONI662IACT
MENTHYL SALICYLATE, (+/-)-43XOA705ZDIACT
SALICYLIC ACIDO414PZ4LPZIACT
THYMOL3J50XA376EIACT
ZINC STEARATEH92E6QA4FVIACT

Source Document#

Source XML · Source PDF

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
3af6617c-2131-49d5-8c3d-99d27cd3c253206cd4f9-5829-41aa-8187-16728bcabfd72016-12-18WarningsExact identifier
spl id: 3af6617c-2131-49d5-8c3d-99d27cd3c253
spl set id: 206cd4f9-5829-41aa-8187-16728bcabfd7

Reported adverse events (FAERS/openFDA)#

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