FDA.reportPublic FDA data

Medicated BODY POWDER Menthol 0.15%

Manufacturer
CVS Pharmacy, Inc.
Effective date
2026-08-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-15 01:00:58

Label at a glance#

ProductMedicated BODY
Active ingredientMENTHOL
Label structure10 sections

Indications and uses

temporary relief of 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#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

temporary relief of pain and itch associated with:
■ minor cuts
■ sunburn
■ insect bites
■ scrapes
■ minor burns
■ minor skin irritations

Warnings

WARNINGS SECTION

■ For external use only
■ Avoid contact with eyes.

OTC - STOP USE SECTION

Stop use and ask a doctor if:
■ condition worsens
■ symptoms persist for more than 7 days or clear up and occur again within a few days

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 right away.

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, Tricalcium Phosphate, Sodium Bicarbonate, Salicylic Acid, Zinc Stearate, Eucalyptus Oil, Peppermint Oil.

SPL UNCLASSIFIED SECTION

†This product is not manufactured or distributed by Chattem Inc., distributor of Gold Bond® Medicated Body Powder.

Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895

NDC 51316-519-10

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

227230_MedicatedBodyPowder_10oz_LBL227230_MedicatedBodyPowder_10oz_LBL

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51316-51951316-519-10

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
STARCH, CORNO8232NY3SJIACT
ZINC OXIDESOI2LOH54ZIACT
TRICALCIUM PHOSPHATEK4C08XP666IACT
SODIUM BICARBONATE8MDF5V39QOIACT
SALICYLIC ACIDO414PZ4LPZIACT
ZINC STEARATEH92E6QA4FVIACT
EUCALYPTUS OIL2R04ONI662IACT
PEPPERMINT OILAV092KU4JHIACT

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
Medicated BODYMENTHOLCVS Pharmacy, Inc.a0f61498-69c8-4ce0-bbd7-3a807f192d362026-08-11WarningsExact identifier
ndc (package): 51316-519-10
ndc (product): 51316-519
ndc11 (package): 51316051910
spl id: 90fb0a8d-acc7-4b71-bdb3-4a3c8b644320
spl set id: a0f61498-69c8-4ce0-bbd7-3a807f192d36

Reported adverse events (FAERS/openFDA)#

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