Body

Manufacturer
CVS Pharmacy, Inc | Vi-Jon, LLC | MK Packaging
Effective date
2021-04-21
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-01 22:46:05

Label at a glance#

ProductBody
Active ingredientMENTHOL
Label structure12 sections

Indications and uses

for temporary relief of pan and itching due to: mnor cuts sunburn insect bites poison ivy poison oak poison sumac scrapes  minor burns minor skin irritations

Dosage and administration

adults and children 2 year of age and older - apply to affected area not more than 3 to 4 times daily children under 2 years of age - do not use, consult 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

for temporary relief of pan and itching due to:

  • mnor cuts
  • sunburn
  • insect bites
  • poison ivy
  • poison oak
  • poison sumac
  • scrapes 
  • minor burns
  • minor skin irritations

warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with the eyes

Stop use and ask a doctor

OTC - STOP USE SECTION

If condition worsens, or if symptoms persist for more than 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

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 year of age and older - apply to affected area not more than 3 to 4 times daily

children under 2 years of age - do not use, consult a doctor

  • for best results dry skin thoroughly before applying

Inactive ingredients

INACTIVE INGREDIENT SECTION

Zea mays (corn) starch, sodium bicarbonate, tricalcium phosphate, zinc oxide, acacia seyal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate

disclaimers

SPL UNCLASSIFIED SECTION

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

This product is sold by weight, not by volume. Some settling may occur during handling and shipping

Adverse Reaction

ADVERSE REACTIONS SECTION

Distributed by: CVS Pharmacy, Inc

One CVS Drive, Woonsocket, RI 02895

2016 CVS/Pharmacy

CVS.com 1-800-SHOP CVS

Made in the U.S.A. with U.S.

and foreign components

379.001/379AB

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BLADE

FOR MEN

MEDICATED

BODY POWDER

EXTERNAL ANALGESIC

ORIGINAL

STRENGTH

PAIN RELIEVING

POWDER

ABSORBS MOISTURE

COOLING

ITCH RELIEVING

Compare to Gold Bond

Medicated Body Powder

CVS

pharmacy

NET WT 10 OZ (283 g)

image descriptionimage description

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
69842-01169842-011-10

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
a02fc26e-4da9-411f-80ae-30ae830a49de4983fa70-bba4-417a-b328-e8ff26abd9bb2022-04-14Warnings, Adverse reactionsExact identifier
spl set id: 4983fa70-bba4-417a-b328-e8ff26abd9bb

Reported adverse events (FAERS/openFDA)#

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