Medicated Body Powder
FDA Label NDC 59240-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Magverz Inc for the product Medicated Body Powder (NDC 59240-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding acitves, inactives, uses, purpose, directions, warning, keep out of reach of childrens, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Acitves

Menthol 0.15%
Zinc Oxide 1.0%

Inactives

Talc
Salicylic Acid
Methyl Salicylate
Eucalyptol
Thymol
Zinc Stearate

Acacia

Uses

Temporarily relieves the pain and itch associated with

Minor cuts

  • Sunburn Insect Bites
  • Scrapes Prickly
  • HeatMinor
  • Burns Rashes
  • Minor Skin Irritations

Purpose

Temporarily relieves the pain and itch

Directions

  • 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.

Warning

For external use only.

When using this product avoid contact with eyes.

Stop use and ask doctor if condition worsens, symptomos do not get better within 7 days.

Keep Out Of Reach Of Childrens

Keep out of reach of childrens.

Product Label

Image Product Label (Bod Owder)

Image Product Label (Bod Owder)

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