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Trilogel

Dosage form
GEL
Labeler
Trifluent Pharma LLC
Label updated
2025-10-14
Retrieved
2026-09-07
Active ingredients
See original label
View original label and images on DailyMed ↗
Label information

Drug Facts

Active Ingredient

Lidocaine HCl, USP 2.8%

Purpose

Topical analgesic

Uses

For the temporary relief of pain associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations.

Warnings

For external use only

Label information

Do not use in large quantities, particularly over raw surfaces or blistered areas.

Label information

When using this product avoid contact with eyes

Label information

Stop use and ask a physician 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 and consult a physician.

Label information

If pregnant or breastfeeding, ask a health professional before use.

Label information

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions
  • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: Do not use; consult a physician.
Other Information

Store at 20-25°C (68-77°F). Protect from freezing.

Inactive Ingredients

Caprylyl Glycol, Carica Papaya (Papaya) Fruit Extract, Disodium EDTA, Ethylhexylglycerin, Glycerin, Hexylene Glycol, Hydroxypropylcellulose, Phenoxyethanol, Purified Water, Sodium Lactate, Xanthan Gum.

Questions or Comments?

(210) 944-6920

PRINCIPAL DISPLAY PANEL - 57 G Pouch Label

Tear at notch to open. Do not use if seal is broken.

NDC: 73352-620-01

TRIFLUENT
PHARMA™

Trilogel™

Lidocaine HCl 2.8%

Topical Analgesic Gel

For the temporary relief of pain associated with minor burns, sunburn,
minor cuts, scrapes, insect bites, and minor skin irritations.

NET WT. 2 OZ. (57 G)

[Image in the official label — see DailyMed source]

DailyMed Set ID: 22af7d63-6a56-4a38-a95b-0f88410b23cb · Version 4
NDC: 73352-620