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Target Up and Up Pain Relief Menthol Topical Analgesic

Dosage form
SPRAY
Labeler
Target Corporation
Label updated
2026-01-23
Retrieved
2026-09-07
Active ingredients
MENTHOL, UNSPECIFIED FORM
View original label and images on DailyMed ↗
Active Ingredient

Menthol 10.5%

Purpose

Pain Relieving Spray

Uses

for the temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains, sprains and bruises

Warnings

For external use only

Flammable: Keep away from excessive heat or open flame

Do not use
  • on wounds or damaged skin
  • on irritated skin
  • with other ointments, creams, sprays or liniments
Ask doctor before use if you have

sensitive skin

When using this product
  • avoid contact with the eyes or mucuous membranes
  • do not bandage tightly
  • do not use with heating pad or device
  • Keep away from face to avoid breathing it
  • do not puncture or incinerate. Contents under pressure.
  • Do not store at temperature above 120 oF
Stop use and ask a doctor if
  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
If pregnant or breastfeeding,

ask a professional before use

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Massage not necessary. Wash hands after use with cool water. Children under 12 years of age: Do not use, consult a doctor

Other information

Store in a cool, dry place

Inactive ingredients

alcohol denat., arnica montana flower extract, calendula officinalis flower extract, camellia sinensis extract, chamomilla recutita (matricaria) flower extract, dimethyl sulfone, echinacea angustifolia extract, glycerin, ilex paraguariensis leaf extract, isopropyl alcohol, isopropyl myristate, juniperus communis fruit extract, purified water

Label

[Image in the official label — see DailyMed source]

DailyMed Set ID: 4910f32f-c639-0215-e063-6394a90a1c7b · Version 1
NDC: 82442-430