FDA.reportPublic FDA data

Walgreens Arthritis Pain Relief Cream

Manufacturer
Walgreens Company
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:38:24

Label at a glance#

ProductWalgreens Arthritis Pain Relief Cream
Active ingredientHISTAMINE DIHYDROCHLORIDE
Label structure12 sections

Indications and uses

For temporary relief of minor aches and pains of muscles and joints assited with arthritis, simple backache, strains & bruises.

Storage and handling

Store between 68° and 77° F ( 20° and 25° C) Tamper evident feature:do not use if outer shrink wrap on jar is torn, broken or missing.

Label contents#

Full prescribing information#

Active Ingredient 

OTC - ACTIVE INGREDIENT SECTION

Histamine Dihydrochloride  0.025% 

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints assited with arthritis, simple backache, strains & bruises.

Warnings

WARNINGS SECTION

For external use only.

Do not use on wounds or damaged skin or if you are allergic to ingredients in the product.

When using this product

OTC - WHEN USING SECTION

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 a doctor if

OTC - STOP USE SECTION

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 adults and Children over 12 years of age.

apply a thin layer to the 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.

Other Information 

STORAGE AND HANDLING SECTION

Store between 68° and 77° F ( 20° and 25° C)

Tamper evident feature:do not use if outer shrink wrap on jar is torn, broken or missing.

Inactive Ingredients 

INACTIVE INGREDIENT SECTION

 Butylene Glycol, C13-C14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethylhexyl Stearate, Glucosamine HCL, Hellanthus Annuus( Sunflower )Oil, Laureth-7, Methylisothiazolinone, Methylsulfonylmethane,Polyacrylamide, Potassium Sorbate, Sodium Polyacrylate, Tetrasodium EDTA,   Tocopheryl Acetate, Trideceth-6, Water (purified)

Principal Display Panel -Jar

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens Arthritis Pain Relief    NDC 0363-5301-40

Histamine Dihydrochloride 0.025%

Arthritis Pain Relief Cream 

NET WT 4OZ (113g)

70020481B_Walgreens_ArthritisPainRelief_4oz_WIC_760245_m115210.jpg70020481B_Walgreens_ArthritisPainRelief_4oz_WIC_760245_m115210.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1091387histamine dihydrochloride 0.025 % Topical CreamPSN4
1091387histamine dihydrochloride 0.25 MG/ML Topical CreamSCD4
1091387histamine dihydrochloride 0.025 % Topical CreamSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-5301-40Walgreens Arthritis Pain Relief Cream113 g in 1 JARCREAM1134

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-5301WALGREENS ARTHRITIS PAIN RELIEF CREAM (HISTAMINE DIHYDROCHLORIDE) CREAM [WALGREENS COMPANY]4Current NDC, Legacy NDC, 1 package rows20241122_80d3031a-7fa9-4f5b-b85e-c7c6ef314801.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-53010363-5301-40

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
BUTYLENE GLYCOL3XUS85K0RAIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
CHONDROITIN SULFATE (SHARK)2ZAJ1K50XHIACT
EMU OIL344821WD61IACT
ETHYLHEXYL STEARATEEG3PA2K3K5IACT
GLUCOSAMINE HYDROCHLORIDE750W5330FYIACT
HELIANTHUS ANNUUS FLOWERING TOPBKJ0J3D1BPIACT
LAURETH-7Z95S6G8201IACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
POLYACRYLAMIDE (1500 MW)5D6TC4BRWVIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
TETRASODIUM EDETATE DIHYDRATE3JGX4KKZ4AIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TRIDECETH-63T5PCR2H0CIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Walgreens Arthritis Pain Relief CreamHISTAMINE DIHYDROCHLORIDEWalgreens Company80d3031a-7fa9-4f5b-b85e-c7c6ef3148012024-11-20WarningsExact identifier
ndc (package): 0363-5301-40
ndc (product): 0363-5301
ndc11 (package): 00363530140
spl id: 6e274c8c-627c-4a48-937b-5304ea400ab9
spl set id: 80d3031a-7fa9-4f5b-b85e-c7c6ef314801

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.