Otc - Active Ingredient
Active ingredient
Pramoxine HCI 1%
Licefreee Afterlice Spray
FDA Label NDC 51879-260
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tec Laboratories Inc. for the product Licefreee Afterlice (NDC 51879-260). 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 otc - active ingredient, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, storage and handling, inactive ingredient, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
For external use only
Otc - When Using
When using this product
- avoid contact with eyes
Otc - Stop Use
Stop use and ask a doctor if
- condition worstens
- 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.
Storage And Handling
Other Information
Store at 59-86°F (15-30°C)
Inactive Ingredient
Inactive ingredients
alcohol, benzethonium CI, menthol, panthenol, polyoxyl 35 castor oil, polyquaternium-10, purified water, tea tree oil
Otc - Questions
Questions or comments?
Call 1-800-482-4464.
Indications & Usage
Uses
for the temporary relief of itching associated with
- insect bites
- minor skin irritations
Dosage & Administration
Directions
- Adults and children 2 years of age and older: spray on affected area not more than 3-4 times daily
- Children under 2 years; do not use; consult a doctor
Otc - Purpose
Pain and itch relief spray for scalp irritation caused by lice bites and lice treatments.
* Please review the disclaimer below.
