Drug Facts
Lidocaine 4%
Greencaine Blast Gel
FDA Label NDC 69747-040
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Alma Laboratories, Inc. for the product Greencaine Blast (NDC 69747-040). 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 drug facts, active ingredient, purpose, uses, warnings, flammable, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Lidocaine 4%
Purpose
Topical Anesthetic
Uses
For the temporary relief of pain and itching associated with minor skin irritations, minor cuts, minor burns, scrapes or insect bites.
Warnings
For external use only
Flammable
Keep away from heat, sparks, electrical, fire or flame.
When Using This Product
avoid contact with the eyes. Do not use in large quantities, particularly over raw surfaces or blistered areas.
Stop Use And Ask A Doctor
if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product.
Keep Out Of The Reach Of Children
If swallowed, get medical helo 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 times daily. Children under 2 years of age consult a doctor.
Inactive Ingredients:
Aloe barbadensis leaf juice (aloe vera), caprylyl glycol, carbomer, disodium EDTA, glycerin, glyceryl laurate, jojoba oil, SD alcohol 40-B, trithanolamine, water.
Questions:
Call (888) 306-6933 or visit www.greencaine.com
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