Active Ingredient
menthol(1%) analgesic, External
Uses
Menthol
FDA Label NDC 70470-1011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Phytopia Co., Ltd. for the product Menthol (NDC 70470-1011). 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, uses, dosage suggestion, directions, inactive ingredient, warning, other information, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Helps relieve the condition of cellulitis infection.
Dosage Suggestion
Adults 10ml maximum per day, Children 5ml maximum per day
Directions
Apply on skin and gentle massage around infected area.
Inactive Ingredient
Thyme Oil, Peppermint Oil, Lemon Oil, Lavender Oil, Geranium Oil (Algerian Type), Olive Oil, Almond Oil, Sunflower Oil, Evening Primrose Oil, Calendula Officinalis Seed Oil.
Warning
- For external use only.
- Stop use and ask doctor if rash occurs.
- Keep out reach of children.
Keep out reach of children.
Other Information
Protect this product from excessive heat and direct sun.
Package Label
All (Otc Label 70470 1011)
* Please review the disclaimer below.
