FDA Label for Ocean Potion Pain Relieving Gel
View Indications, Usage & Precautions
Ocean Potion Pain Relieving Gel Product Label
The following document was submitted to the FDA by the labeler of this product Prime Enterprises. 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 Ingredients
Lidocaine Hydrochloride 0.72%
Purpose
Topical Anesthetic
Uses
- for the temporary relief of pain and itching associated with sunburn, minor burns, minor skin irritations, scrapes, insect bites
Warnings
For exeternal use only
Do Not Use
in large quantities, particularly over raw surfaces or areas with blisters
When Using This Product
- avoid contact with eyes
- use only as directed
Stop Use And Consult A Doctor If
- condition worsens, or symptoms last more than 7 days
- symptoms clear up and occur again within a few days
Keep Out Of Reach Of Children
- if swallowed, get medical help or contact a Poison Control Center right away
- Certain persons can develop allergic reactions to ingredients in this product. If symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase, discontinue use and consult a doctor
Directions
- Adults and children 2 years or older: apply to affected area not more than 3 - 4 times daily
- Children under 2 years of age: do not use, ask a doctor
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Blue 1, Carbomer, Disodium EDTA, Ethylhexylglycerin, Fragrance, Menthol, Phenoxyethanol, Polysorbate 20, Propylene Glycol, SD Alcohol 40-B, Sodium Hydroxide, Water, Yellow 5
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