Real Time Pain Relief MAXXTopical Analgesic
- Dosage form
- LOTION
- Labeler
- Cosmetic Specialty Labs, Inc.
- Label updated
- 2020-02-10
- Retrieved
- 2026-09-07
- Active ingredients
- MENTHOL
Label information
Drug Facts
Active Ingredient
Menthol 1.5%
Purpose
Topical analgesic
Uses
temporarily relieves minor pain associated with:
- arthritis
- simple backache
- muscle strains
- sprains
- bruises
- cramps
Warnings
for external use only
When using this product
- use only as directed
- avoid contact with eyes or mucous membranes
- do not apply to wounds or damaged skin
- do not bandage tightly
Stop use and ask a doctor if
- condition worsens
- symptoms persist for more than 7 days or clear up and occur again within a few days
- redness is present
- irritation develops
Label information
If pregnant or breast-feeding, 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 right away.
Directions
adults and children over 2 years:
- apply generously to affected area
- massage into painful area until thoroughly absorbed into skin
- repeat as necessary, but no more than 4 times daily
children 2 years or younger: ask a doctor
Inactive ingredients
Aloe Barbadensis Leaf, Anthemis nobilis, Arnica Montana Flower Extract, Butylene Glycol, Calendula officianlis, Caprylyl Glycol, Capsicum Frutescens Fruit, Carbomer, Centaurea cyanus, Cetearyl Alcohol, Cetyl Alcohol, Coriandrum Sativum (Coriander) Fruit Oil, Diazolidinyl Urea, Emu Oil, Glucosamine HCI, Hamamelis Virginiana (Witch Hazel) Bark/Leaf/Twig Extract, Hypericum perforatum, Matricaria chamomilla, Mentha Piperita (Peppermint) Leaf Oil, Methylsulfonylmethane, Phenoxyethanol, Purified Water, Salix Alba (Willow) Bark Extract, SD Alcohol 40, Sodium Chondroitin Sulfate, Sorbitol, Tilia cordata, Triethanolamine.
Label information
Distributed by: RTPR LLC, Edmond, OK 73012
PRINCIPAL DISPLAY PANEL - 120 mL Label
[Image in the official label — see DailyMed source]
DailyMed Set ID: 6180d7e4-1bc5-ffc5-e053-2991aa0af1b9 · Version 3
NDC: 58133-100