MedPride Medicated Body Powder

Manufacturer
Shield Line LLC
Effective date
2025-08-15
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:11:33

Label at a glance#

ProductMedPride Medicated Body Powder 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 Facts Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.15 %

Zinc Oxide 1.0%

Purpose

OTC - PURPOSE SECTION

Anti-itch

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.
  • Keep away from face and mouth to avoid inhalation
  • 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

Corn Starch, Eucalyptol, Gum Talha, Methyl Salicylate, Salicylic Acid, Sodium Bicarbonate, Thymol, Tricalcium Phosphate, Zinc Stearate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display and Drug Fact PanelPrincipal Display and Drug Fact Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
577232menthol 0.15 % / zinc oxide 1 % Topical PowderPSN6
577232menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical PowderSCD6
577232Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical PowderSY6
577232menthol 0.15 % / zinc oxide 1 % Topical PowderSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52410-4031-02023-07-31C16284748780-1f386c64a-3818-0266-e053-dadaa90a7c1aMedPride Medicated Body Powder
52410-4031-02023-01-30C16284748780-1f386c64a-3818-0266-e053-dadaa90a7c1aMedPride Medicated Body Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52410-4031-0MedPride Medicated Body PowderPowder283 g in 1 BOTTLEPOWDER2836

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52410-403152410-4031-0

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
MedPride Medicated Body Powder PowderMENTHOL, ZINC OXIDEShield Line LLCcdb2fa5b-cf04-c876-e053-2a95a90a187c2025-08-15WarningsExact identifier
ndc (package): 52410-4031-0
ndc (product): 52410-4031
ndc11 (package): 52410403100
spl id: 3c6f2a69-2780-e22a-e063-6294a90ad4ab
spl set id: cdb2fa5b-cf04-c876-e053-2a95a90a187c

Reported adverse events (FAERS/openFDA)#

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