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Drug Facts
Lotrimin Daily Sweat And Odor Control Powder
FDA Label NDC 11523-0012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bayer Healthcare Llc. for the product Lotrimin Daily Sweat And Odor Control (NDC 11523-0012). 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 other, otc - active ingredient, otc - purpose, use, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active ingredient
Topical starch 83.7%
Otc - Purpose
Purpose
Skin Protectant
Use
Use
temporarily protects and helps relieve minor skin irritation
Warnings
Warnings
For external use only
Otc - Do Not Use
Do not use on broken skin.
Otc - When Using
When using this product
• Do not get into eyes
• Keep away from face and mouth to avoid breathing it
Otc - Stop Use
Stop use and ask a doctor if
- Condition worsens
- Symptoms last more than 7 days or clear up and occur again within a few days
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions
Apply as needed
Inactive Ingredient
Inactive ingredients
benzethonium chloride;camphor (synthetic);eucalyptus oil;kaolin;lemon oil;zinc oxide
Questions
Questions? 1-866-360-3266
Package Display
LOTRIMIN
TOPICAL STARCH SKIN PROTECTANT
medicated foot powder
DAILY SWEAT
& ODOR CONTROL
6 odor-fighting
ingredients to control odor
- super sweat absorbent powder
- relieves irritation
- talc-free
NET WT 177 G (6.25 OZ)
* Please review the disclaimer below.
