OTC - ACTIVE INGREDIENT SECTION
Histamine Dihydrochloride 0.025%
Walgreens - Arthritis Pain Relief Cream
- Manufacturer
- Walgreens
- Effective date
- 2024-12-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:46:57
Label at a glance#
ProductArthritis Pain Relief
Active ingredientHISTAMINE DIHYDROCHLORIDE
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Topical Analgesic
INDICATIONS & USAGE SECTION
For temporary relief of minor aches and pains of muscles and joints associated with arthritis, simple backache, strains & bruises.
WARNINGS SECTION
For external use only
OTC - DO NOT USE SECTION
Do not use on wounds or damaged skin or if you are allergic to ingredients in the products
OTC - WHEN USING SECTION
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.
OTC - STOP USE SECTION
Stop use and ask a 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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast- feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
For Use by Adult and Children over 12 years of age.
Apply a thin layer to the pain site and message until thoroughly absorbed into skin.
Apply no more than 3 to 4 times daily.
Children 12 years or younger consult a physician
OTHER SAFETY INFORMATION
Store between 68°C and 77° F (20° and 25° C)
INACTIVE INGREDIENT SECTION
Acrylates/Acrylamide Copolymer )and) Mineral Oil (and) Polysorbate 85, Cetyl Alcohol, Chondroitin Sulfate, Dimethicone, disodium EDTA, Emu Oil, Glucosamine HCl, Glycerin, Helianthus Annus (Sunflower) Extract, Isopropyl Palmitate, Methyl Sulfonyl Methane (MSM), Phenoxyethanol, Propylene Glycol, Stearic Acid, Tocopheryl Actate, Triethanolamine, Water
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Arthritis Pain Relief
- Histamine Dihydrochloride .025%
- GLUCOSAMINE HYDROCHLORIDE
- STEARIC ACID
- EMU OIL
- HELIANTHUS ANNUUS FLOWERING TOP
- PHENOXYETHANOL
- HISTAMINE DIHYDROCHLORIDE
- HISTAMINE
- WATER
- PROPYLENE GLYCOL
- CETYL ALCOHOL
- TROLAMINE
- .ALPHA.-TOCOPHEROL ACETATE
- EDETATE DISODIUM ANHYDROUS
- GLYCERIN
- ISOPROPYL PALMITATE
- DIMETHICONE
- CHONDROITIN SULFATE (PORCINE)
- MINERAL OIL
- DIMETHYL SULFONE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0363-3035 | 0363-3035-25 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 471aee63-dbe7-e107-e063-6294a90ad200 | ce16e74c-e5c7-5c4d-e053-2a95a90a72a7 | 2025-12-29 | Warnings | ce16e74c-e5c7-5c4d-e053-2a95a90a72a7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.