FDA Label for Foot Hangover
View Indications, Usage & Precautions
Foot Hangover Product Label
The following document was submitted to the FDA by the labeler of this product Ari Brands, Llc. 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.
Drug Facts
Active Ingredients (In Each Bottle)
Lidocaine HCL 4%
Purpose
External analgesic
Uses
For the temporary relief of pain and itching due to minor burns, sunburn, minor cuts, abrasions, insect bites, and minor skin irritations.
Warnings
For external use only. Avoid contact with eyes.
Flammable: Do not use while smoking or near heat or flame.
Do not use in large quantities, particularly over raw surfaces or blistered areas, on large areas of the body or on a cut, irritated or swollen skin, or for more than one week without consulting a physician.
Stop use and ask a doctor if: conditions worsen, symptoms persist for more than 7 days or clear up and occur again within a few days.
If pregnant or breast feeding, ask a health professional before use.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children and pets. If swallowed, get medical help or contact the Poison Control Center right away.
Dosage & Administration
| Directions | |
| adults and children 2 years and older | apply externally to the affected area up to 3 to 4 times a day |
| children under 2 years | ask a doctor |
Other Information
Contents under pressure. Do not store at temperatures above 120° F
When using this product; Use only as directed. Do not puncture or incinerate.
Inactive Ingredients
Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Distilled water), Parfum (Fragrance), Potassium Sorbate, Saccharide Isomerate, SD-Alcohol 40B
Packaging
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