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NDC 00363-5301-40 Walgreens Arthritis Pain Relief Cream 0.00025 g/g Details

Walgreens Arthritis Pain Relief Cream 0.00025 g/g

Walgreens Arthritis Pain Relief Cream is a TOPICAL CREAM in the HUMAN OTC DRUG category. It is labeled and distributed by Walgreens Company. The primary component is HISTAMINE DIHYDROCHLORIDE.

Product Information

NDC	00363-5301
Product ID	0363-5301_07a99cc9-cf5b-4f2e-a857-396699d62024
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Walgreens Arthritis Pain Relief Cream
Proprietary Name Suffix	n/a
Non-Proprietary Name	Histamine Dihydrochloride
Product Type	HUMAN OTC DRUG
Dosage Form	CREAM
Route	TOPICAL
Active Ingredient Strength	0.00025
Active Ingredient Units	g/g
Substance Name	HISTAMINE DIHYDROCHLORIDE
Labeler Name	Walgreens Company
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00363-5301-40 (00363530140)

Pricing Information	N/A
NDC Package Code	0363-5301-40
Billing NDC	00363530140
Package	113 g in 1 JAR (0363-5301-40)
Marketing Start Date	2022-04-30
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 80d3031a-7fa9-4f5b-b85e-c7c6ef314801 Details

Drug Fact

Active Ingredient

Histamine Dihydrochloride 0.025%

Purpose

Topical Analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints assited 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 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 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.

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED SECTION

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

SPL UNCLASSIFIED 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

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

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

Walgreens Arthritis Pain Relief NDC 0363-5301-40

Histamine Dihydrochloride 0.025%

Arthritis Pain Relief Cream

NET WT 4OZ (113g)

INGREDIENTS AND APPEARANCE

WALGREENS ARTHRITIS PAIN RELIEF CREAM

histamine dihydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0363-5301
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	0.00025 g in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0363-5301-40	113 g in 1 JAR; Type 0: Not a Combination Product	04/30/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	04/30/2022

Labeler - Walgreens Company (008965063)

Revised: 4/2022

Document Id: 07a99cc9-cf5b-4f2e-a857-396699d62024

Set id: 80d3031a-7fa9-4f5b-b85e-c7c6ef314801

Version: 3

Effective Time: 20220427

Search by Drug Name or NDC

NDC 00363-5301-40 Walgreens Arthritis Pain Relief Cream 0.00025 g/g Details

Walgreens Arthritis Pain Relief Cream 0.00025 g/g

Product Information

Package

Package Images

NDC 00363-5301-40 (00363530140)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 80d3031a-7fa9-4f5b-b85e-c7c6ef314801 Details

Drug Fact

Active Ingredient

Purpose

Uses

Warnings

When using this product

Stop use and ask a doctor if

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

Other Information

Inactive Ingredients

Principal Display Panel -Jar

INGREDIENTS AND APPEARANCE

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