Label: HISTAMINE DIHYDROCHLORIDE cream
- NDC Code(s): 83088-8120-8
- Packager: USA Hemp Store LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
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- Broadway Joe's Pain Cream
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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
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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
- Broadway Joe's Pain Cream
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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 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.
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
- Broadway Joe's Pain Cream
- Broadway Joe's Pain Cream
- Broadway Joe's Pain Cream
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INGREDIENTS AND APPEARANCE
HISTAMINE DIHYDROCHLORIDE
histamine dihydrochloride creamProduct 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:83088-8120-8 14.8 mL in 1 JAR; Type 0: Not a Combination Product 02/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/01/2023 Labeler - USA Hemp Store LLC (036959608) Registrant - Lexia LLC (050186540) Establishment Name Address ID/FEI Business Operations Lexia LLC 015552120 manufacture(83088-8120)
