Active Ingredient
Benzocaine, 20%
The following Structured Product Label (SPL) was submitted to the FDA by Dharma Research, Inc. for the product Ioline (NDC 53045-137). 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 active ingredient, purpose, uses, warnings, otc - do not use, other, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Benzocaine, 20%
Oral anesthetic
For the temporary relief of pain associated with canker sores and minor dental procedures.
Alergy alert. Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "-caine" anesthetics.
Do not use this product for more than 7 days unless directed by a dentist or doctor. If sore mouth symptoms do not improve in 7 days; if irritation, pain, or redness persists or worsens; or if swelling, rash, or fever develops, see your dentist or doctor promptly.
Do not exceed recommended dosage.
Keep Out of Reach of Children. If more than used for pain is accidentially swallowed, get medical help or contact a Poison Control center right away.
Store at room temperature 59-86°F (15-30°C). Protect from freezing and heat.
FD&C Red #40, FD&C Blue #1, FD&C Yellow #6, FD&C Yellow #5, Flavor, Polyethylene glycol 3350, Polyethylene glycol 400, Saccharine sodium, Tocopheryl acetate, Xylitol
Oral Anesthetic Gel Pina Colada
with Vitamin E and Xylitol
Gluten Free
1.12 oz (32 g)
Manufactured by Dharma Research, Inc., 5220 NW 72nd Ave, Unit 15, Miami, FL 33166
1-877-833-3725
www.dharmaresearch.com
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