TheraCare Roll-on Lidocaine Pain Relief Liquid - Lavender
- Dosage form
- LIQUID
- Labeler
- Veridian Healthcare
- Label updated
- 2025-09-18
- Retrieved
- 2026-09-07
- Active ingredients
- LIDOCAINE
Label information
TheraCare Roll-on Lidocaine Pain Relief Liquid- Lavender
Active ingredient
Lidocaine 4%
Purpose
Topical analgesic
Uses
temporarily relieves minor pain
Warnings
For external use only
When using this product
- use only as directed. Read and follow all directions and warnings on this carton.
- do not allow contact with the eyes and mucus membranes
- do not bandage tightly or apply local heat (such as heating pads) or a medicated patch to the area of use
- do not use at the same time as other topical analgesics
Stop use and ask a doctor if
- condition worsens
- redness is present
- irritation develops
- symptoms persist for more than 7 days or clear up and occur again within a few days
Flammable■ Keep away from fire or flame
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
adults and children over 12 years:
- apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24-hour period
children 12 years or younger:ask a doctor
Inactive ingredients
Inactive ingredients acrylates/C10-30 alkyl acrylate crosspolymer (60000 MPA.S), aloe barbadensis leaf juice, aminomethylpropanol,
ceteth-10 phosphate, cetostearyl alcohol, cyclomethicone 5, dihexadecyl phosphate, dimethicone 350, dimethicone/vinyl dimethicone
crosspolymer (soft particle), edetate disodium anhydrous, ethylhexylglycerin, glyceryl 1-stearate, hydroxyethyl acrylate/sodium
acryloyldimethyl taurate copolymer (100000 MPA.S at 1.5%), isohexadecane, lavandula angustifolla (lavender) oil, phenoxyethanol, SD
alcohol, steareth-21, water
Questions or comments
Call 1-866-326-1313
Principal Display Panel
[Image in the official label — see DailyMed source]
DailyMed Set ID: 6bebce76-30f6-4070-b0fe-58246d071328 · Version 1
NDC: 71101-088