FDA Label for Leader After Sun Cooling
View Indications, Usage & Precautions
Leader After Sun Cooling Product Label
The following document was submitted to the FDA by the labeler of this product Cardinal Health, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Lidocaine hydrochloride 0.5%
Purpose
External Analgesic
Uses
temporarily relieves pain and itching due to:
- minor skin irritations
- sunburn
- minor burns
- scrapes
- minor cuts
- insect bites
Warnings
- For External Use Only
Otc - Do Not Use
Do not use in large quantities, particularly over raw surfaces or blistered areas.
Otc - When Using
When using this product
- Avoid contact with eyes. If contact occurs, rinse with water to remove.
Otc - Ask Doctor
Stop use and ask a doctor if
- condition gets worse
- symptoms last more than 7 days
- symptoms clear up and occur again in 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
- adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.
- children under 2 years of age: ask a doctor
Other Safety Information
Other information may stain some fabrics
Inactive Ingredients
aloe barbadensis leaf juice, water, isopropyl alcohol, propylene glycol, glycerin, triethanolamine, carbomer, polysorbate 80, diazolidinyl urea, menthol, disodium EDTA, yellow 5, blue 1
Questions Or Comments?
Call toll free 1-800-527-7731
Package Label.Principal Display Panel
Leader After Sun Cooling Gel
NET WT 8 OZ (226 g)
NDC 70000-0534-1
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