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Phoenix KinetiCream Anti-inflammatory and Pain Relief

Dosage form
CREAM
Labeler
Pure Source, LLC
Label updated
2023-11-05
Retrieved
2026-09-07
Active ingredients
MENTHOL
View original label and images on DailyMed ↗
Active Ingredients

Menthol 2.00%

Purpose

Topical Pain Relief

Uses

temporary relieves of these symptoms:

  • minor aches
  • pains associated with simple backache
  • arthritis
  • bruises
  • sprains
  • cramps
  • muscle strains.
Warnings

For external use only.

  • Use only as directed children under 6 years, ask a doctor.

Stop use and ask a doctor if:

  • condition worsen
  • pain persist of more than 7 days
  • irritation develops

Avoid contact with eyes and open wounds.

If swallowed, get medical help or contact your local Poison Control Center or emergency room immediately.

If pregnant or breast feeding

ask a health professional before use.

Keep out of reach of children.

Directions

Adults and children 6 years and over:

  • Before activity, massage onto muscles and joints until absorbed into skin.
  • After activity, apply generously to tired and affected areas
  • Apply to dry and cleans areas
  • Repeat as needed, up to 6 times daily.
Inactive ingredients:

Aloe barbadensis (aloe vera gel) juice, aqua (deionized water), arnica montana (arnica) extract, azadirachta indica (neem) oil, bromelain, butyrospermum parkii (shea) butter, C13-14 isoparaffin, camellia sinensis (green tea) leaf extract, cetearyl alcohol, chondroitin sulfate, citric acid, citrus aurantium bergamia (bergamot) fruit oil, dimethyl sulfone (MSM), emu oil, ethylhexylglycerin, glucosamine sulfate, glycerin, glyceryl stearate SE, laureth-7, mentha piperita (peppermint) oil, papain, phenoxyethanol, polyacrylamide, polysorbate-20, salix alba (willow) bark extract, SD-Alcohol 40B, sesamum indicum (sesame) seed oil, stearic acid, theobroma cacao (cocoa butter), tocopheryl acetate (vitamin E), xanthan gum.

Package Labeling:

[Image in the official label — see DailyMed source]

DailyMed Set ID: c28cd0d6-8db8-425b-9790-f396f76dc7ac · Version 9
NDC: 65121-032