Label: WALGREENS ARTHRITIS PAIN RELIEF CREAM- histamine dihydrochloride cream
- NDC Code(s): 0363-5301-40
- Packager: Walgreens Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2024
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- Drug Fact
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- Other Information
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Inactive Ingredients
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
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INGREDIENTS AND APPEARANCE
WALGREENS ARTHRITIS PAIN RELIEF CREAM
histamine dihydrochloride creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-5301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE 0.00025 g in 1 g Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH) EMU OIL (UNII: 344821WD61) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) LAURETH-7 (UNII: Z95S6G8201) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) TETRASODIUM EDETATE DIHYDRATE (UNII: 3JGX4KKZ4A) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIDECETH-6 (UNII: 3T5PCR2H0C) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-5301-40 113 g in 1 JAR; Type 0: Not a Combination Product 04/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/30/2022 Labeler - Walgreens Company (008965063)