HISTAMINE DIHYDROCHLORIDE cream

histamine dihydrochloride by

Drug Labeling and Warnings

histamine dihydrochloride by is a Otc medication manufactured, distributed, or labeled by USA Hemp Store LLC, Lexia LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Broadway Joe's Pain Cream

Histamine dihydrochloride

Braodway Joe's Pain Cream

Water, Glyceryl Stearate, Caprylic/Capric, Triglyceride, Cetyl Alcohol, Butylene Glycol, Cannabidiol, Cetearyl 2- thylhexanoate, Sodium Hyaluronate, Glycerin, Tapioca Starch, Polymethylsilsesquioxane, Stearic Acid, Cannabis Sativa (Hemp) Seed Oil, 3-glyceryl Ascorbate (Vitamin C), Isonononyl Isononanoate, Tocopheryl Acetate (Vitamin E), Dimethicone, Polysorbate 80, Carbomer, Sodium Hydroxide, Caprylyl Glycol, Phenoxyethanol, Hexylene Glycol

Broadway Joe's Pain Cream

• For use by adults and children over 13 yrs old.
• Gently massage the product on to clean dry skin as needed.
• For topical use only, do not ingest.
• Provides temporary relief from aches and pains associated with simple backaches,strains, sprains, arthritis, bruises.
• Apply a thin layer to pain site and massage until thoroughly absorbed into skin.

Broadway Joe's Pain Cream

Topical Analgesic

Broadway Joe's Pain Cream

Store between 40 degrees F and 86 degrees F (4 degrees C and 30 degrees C).

Broadway Joe's Pain Cream

Warnings· For external use only.
Do not use on open wounds or damaged skin or with a heating pad.

When using this product· avoid contact with eyes or mucous membranes. If product contacts your eyes, rinse thoroughly with water. Do not bandage tightly. · Do not use with other ointments, creams, or sprays.

Stop use and ask a doctor ifyou experience redness or excessive skin irritation over the affected area. · If the condition worsens, or symptoms persist for more than 7 days please consult a Dr.

Keep out of reach of children. If swallowed, seek medical help, or contact a Poison Control Center immediately.

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

Broadway Joe's Pain Cream

Stop use and ask a doctor if you experience redness or excessive skin irritation over the affected area. · If the condition worsens,
or symptoms persist for more than 7 days, please consult a Dr.

Broadway Joe's Pain Cream

Topical Analgesic

Broadway Joe's - 2oz

Keep out of reach of children. If swallowed, seek medical help or contact a poison control center immediately.

Broadway Joe's Pain Cream

INGREDIENTS AND APPEARANCE

HISTAMINE DIHYDROCHLORIDE 
histamine dihydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83088-8120
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 mL

Inactive Ingredients
Ingredient Name	Strength
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARIC ACID (UNII: 4ELV7Z65AP)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
CANNABIDIOL (UNII: 19GBJ60SN5)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
HYALURONIC ACID (UNII: S270N0TRQY)
3-GLYCERYL ASCORBATE (UNII: 3R1Q5X5GGO)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER (UNII: EPA1872R1N)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL DICAPRATE (UNII: 3Z317CA098)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
CETEARYL OLIVATE (UNII: 58B69Q84JO)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Product Characteristics
Color	white (Cream)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83088-8120-6	118 mL in 1 JAR; Type 0: Not a Combination Product	10/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/03/2022

Labeler - USA Hemp Store LLC (036959608)

Registrant - Lexia LLC (050186540)

Establishment
Name	Address	ID/FEI	Business Operations
Lexia LLC		015552120	manufacture(83088-8120)