Medicated Body

Manufacturer: Walmart Stores Inc
Effective date: 2026-02-12
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:44:23

Label at a glance#

ProductMedicated Body Powder

Active ingredientMENTHOL

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 of age and over, apply freely up to 3 or 4 times daily Children under 2 years: consult a physician for best results, dry skin thoroughly before use

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Drug Facts Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15 %

Purpose

OTC - PURPOSE SECTION

External Analgesic

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.

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
Redness, irritation, swelling or pain persist or increases
symptoms do not get better within 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years of age and over, apply freely up to 3 or 4 times daily
Children under 2 years: consult a physician
for best results, dry skin thoroughly before use

Inactive Ingredients

INACTIVE INGREDIENT SECTION

acacia seyl gum, eucalyptol, methyl salicylate, salicylic acid, sodium bicarbonate, thymol, tricalciun phosphate, zea mays (corn stach), zinc oxide, zinc stearate

Equate Medicated Body Powder Original

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

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 Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79903-724-01	Medicated BodyPowder	283 g in 1 BOTTLE	POWDER	283		5
79903-724-04	Medicated BodyPowder	113 g in 1 BOTTLE	POWDER	113		5

Products#

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

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

Medicated Body Powder
MENTHOL
SODIUM BICARBONATE
TRICALCIUM PHOSPHATE
ACACIA
EUCALYPTUS OIL
MENTHYL SALICYLATE, (+/-)-
SALICYLIC ACID
THYMOL
ZINC STEARATE
ZINC OXIDE
ZEA MAYS WHOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79903-724	79903-724-01, 79903-724-04

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
SODIUM BICARBONATE	8MDF5V39QO	IACT
TRICALCIUM PHOSPHATE	K4C08XP666	IACT
ACACIA	5C5403N26O	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
MENTHYL SALICYLATE, (+/-)-	43XOA705ZD	IACT
SALICYLIC ACID	O414PZ4LPZ	IACT
THYMOL	3J50XA376E	IACT
ZINC STEARATE	H92E6QA4FV	IACT
ZINC OXIDE	SOI2LOH54Z	IACT
ZEA MAYS WHOLE	1G5HNE09V8	IACT
MENTHOL	L7T10EIP3A	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
4	2026-01-18	monthly-update	2026-06-03 17:52:55

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
Medicated Body Powder	MENTHOL	Walmart Stores Inc	afd337b7-d76e-f17a-e053-2a95a90abac7	2026-02-12	Warnings	Exact identifier ndc (package): 79903-724-01 ndc (package): 79903-724-04 ndc (product): 79903-724 ndc11 (package): 79903072401 ndc11 (package): 79903072404 spl id: 4aa54023-05f2-2e12-e063-6294a90a6691 spl set id: afd337b7-d76e-f17a-e053-2a95a90abac7

Reported adverse events (FAERS/openFDA)#

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