Hand and Wrist Pain Cream
- Dosage form
- CREAM
- Labeler
- Sombra Cosmetics, Inc.
- Label updated
- 2019-12-09
- Retrieved
- 2026-09-07
- Active ingredients
- HISTAMINE DIHYDROCHLORIDE
Active Ingredients
Histamine Dihydrochloride 0.025%
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away
PURPOSE
PURPOSE
Topical Analgesic
Uses
For temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and bruises
Warnings
For external use only. Do not use on wounds or damaged skin or if you are allergic to ingredients in this product. When using this product: avoid contact with eyes. If product gets into eyes, rinse thoroughly with water. Do not bandage tightly or use a heating pad.
Stop use and ask doctor if: rash appears. Condition worsens. If symptoms persist for more than 7 days or if symptoms clear up and occur again within a few days.
If pregnant or breast feeding, ask a health professional before use.
Directions
For Use by Adults and Children over 12 years. Apply a thin layer to pain site and massage until thoroughly absorbed into skin. Apply no more than 3 to 4 times daily.
Children 12 years or younger consult a physician
Inactive Ingredients
Aloe Barbadensis Leaf (Aloe Vera Gel), Aqua (Purified Water), Ascorbic Acid (Vitamin C), Butylene Glycol, Camellia Sinensis (Green Tea) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Emu Oil, Ethylhexylglycerin, Ethylhexyl Stearate, Glycyrrhiza Glabra (Licorice) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, C13-14 Isoparaffin, Laureth-7, Magnesium Sulfate, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Potassium Sorbate, Purica Granatum (Pomegranate) Extract, Saccharide Isomerate, Sodium Polyacrylate, Tochopheryl Acetate (Vitamin E), Trideceth-6, Vaccinium Angustifolium (Blueberry) Fruit Extract, Zemea (Corn) Propanediol
Questions or Comments?
Call 1-888-600-4642
Label
[Image in the official label — see DailyMed source]
DailyMed Set ID: 49b35ba4-ecb0-4016-94b8-5351fbda8c26 · Version 1
NDC: 61577-8122