Active Ingredient
Menthol 0.15%
Gold Bond Medicated Original Strength Body Powder
FDA Label NDC 67751-225
9 label sections · Submitted to the FDA by Navajo Manufacturing Company Inc. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Navajo Manufacturing Company Inc. for the product Gold Bond Medicated Original Strength Body (NDC 67751-225). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-itch
Uses
temporarily relieves the pain and itch associated with:
■ minor cuts ■ sunburn ■ insect bites ■ scrapes ■ minor burns ■ minor skin irritations
Warnings
For external use only
When Using This Product
■ avoid contact with eyes
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
■ redness, irritation, swelling or pain persists or increases
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center immediately.
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
Inactive Ingredients
zea mays (corn) starch, zinc oxide, acacia senegal gum, silica, tricalcium phosphate, eucalyptol, methyl salicylate, salicylic acid, zinc stearate, thymol
* Please review the disclaimer below.
