ARTHRITIS PAIN RELIEF- histamine dihydrochloride .025% cream

Arthritis Pain Relief by

Drug Labeling and Warnings

Arthritis Pain Relief by is a Otc medication manufactured, distributed, or labeled by Walgreens. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Histamine Dihydrochloride 0.025%

PURPOSE

Topical Analgesic

INDICATIONS & USAGE

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

WARNINGS

For external use only

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

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 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.

If pregnant or breast- feeding, ask a health professional before use.

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ARTHRITIS PAIN RELIEF 
histamine dihydrochloride .025% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-3035
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	0.025 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
STEARIC ACID (UNII: 4ELV7Z65AP)
EMU OIL (UNII: 344821WD61)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETYL ALCOHOL (UNII: 936JST6JCN)
TROLAMINE (UNII: 9O3K93S3TK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CHONDROITIN SULFATE (PORCINE) (UNII: V5E8ELO4W9)
MINERAL OIL (UNII: T5L8T28FGP)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-3035-25	1 in 1 CARTON	11/01/2022
1		113 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	11/01/2022

Labeler - Walgreens (008965063)