Label: HEMPVANA MAXIMUM STRENGTH PAIN RELIEF CREAM 10% TROLAMINE SALICYLATE- trolamine salicylate cream
- NDC Code(s): 73287-032-01
- Packager: TELEBRANDS CORP
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 5, 2025
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
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Warnings
For external use only
Allergy alert:If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.
When using this product
- Use only as directed. Read and follow all directions and warnings on this label.
- Do not bandage tightly or apply local heat (such as heating pads) to the area of use.
- Avoid contact with eyes or mucous membranes.
- Do not apply to wounds or damaged, broken, or irritated skin.
- Do not use at the same time as other topical analgesics.
- Directions
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Inactive Ingredients
Water/Aqua/Eau, Ethylhexyl Stearate,Butylene Glycol, Dimethicone, Stearic Acid, Caprylic/CapricTriglyceride, Glyceryl Stearate, Hemp (Cannabis Sativa) Seed Oil,PEG-100 Stearate, Cetearyl Alcohol, Magnesium Sulfate, Sunflower(Helianthus Annuus) Seed Oil, Allantoin, Acrylates/C10-30 AlkylAcrylate Crosspolymer, Tocopheryl Acetate, Sodium Acrylate/SodiumAcryloyldimethyl Taurate Copolymer, Caprylyl Glycol, Isohexadecane, Hexylene Glycol, Ethylhexylglycerin, Sodium Hydroxide,Polysorbate 80, Disodium EDTA, Phenoxyethanol
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INGREDIENTS AND APPEARANCE
HEMPVANA MAXIMUM STRENGTH PAIN RELIEF CREAM 10% TROLAMINE SALICYLATE
trolamine salicylate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73287-032 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TROLAMINE SALICYLATE (UNII: H8O4040BHD) (SALICYLIC ACID - UNII:O414PZ4LPZ) TROLAMINE SALICYLATE 10 g in 100 g Inactive Ingredients Ingredient Name Strength MAGNESIUM SULFATE (UNII: DE08037SAB) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) CAPRYLYL GLYCOL (UNII: 00YIU5438U) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SODIUM HYDROXIDE (UNII: 55X04QC32I) SUNFLOWER OIL (UNII: 3W1JG795YI) WATER (UNII: 059QF0KO0R) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PEG-100 STEARATE (UNII: YD01N1999R) STEARIC ACID (UNII: 4ELV7Z65AP) ALLANTOIN (UNII: 344S277G0Z) HEXYLENE GLYCOL (UNII: KEH0A3F75J) DIMETHICONE (UNII: 92RU3N3Y1O) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) CETEARYL ALCOHOL (UNII: 2DMT128M1S) ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) (UNII: YY2HMJ9NZF) ISOHEXADECANE (UNII: 918X1OUF1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73287-032-01 1 in 1 CARTON 02/01/2025 1 85 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 Drug M017 02/01/2025 Labeler - TELEBRANDS CORP (177266558) Establishment Name Address ID/FEI Business Operations Neutraderm, Inc. 146224444 manufacture(73287-032)


