Active Ingredients
Benzalkonium Chloride 0.13%
Lidocaine Hydrchloride 2%
Cicloferon Gel
FDA Label NDC 59208-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Liomont, S.a. De C.v. for the product Cicloferon (NDC 59208-002). 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 ingredients, purpose, uses, warnings, do not use, when using this product, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical antiseptic
Topical analgesic
Uses
- provides temporary relief of pain associated with cold sores and fever blisters
- first aid to help protect against infection in minor cuts, scrapes, burns
Warnings
For external use only:
Do not use in the eyes or apply over large areas of the body. In case of deep puncture wounds, animal bites, or serious burns, consult a doctor.
Do Not Use
- for more than 7 days unless told to do so by a doctor
- more than directed
- if you are allergic to any ingredient in this product
When Using This Product
- avoid contact with the eyes
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- clean the affected area
- apply a small amount of this product to the affected area 1 to 3 times daily
- may be covered with a sterile bandage
- children under 12 years of age, consult a doctor
Other Information
- store at 20° to 25°C (68° to 77°F)
Inactive Ingredients
hypromellose, methylparaben, propylene glycol, water, polysorbate 80
Package Label
Package Label (Ciclofrnlbl)
* Please review the disclaimer below.
