Label: HEMPVANA MAXIMUM STRENGTH PAIN RELIEF- trolamine salicylate lotion
- NDC Code(s): 73287-022-01
- Packager: TELEBRANDS CORP
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
-
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
-
Inactive Ingredients
Water/Aqua/Eau, Ethylhexyl Stearate, Butylene Glycol, Caprylic/Capric Triglyceride, Dimethicone, Cannabis Sativa (Hemp) Seed Oil, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Stearic Acid, Tocopheryl Acetate, Allantoin, Phenoxyethanol, Xanthan Gum, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Disodium EDTA, Citric Acid, Sodium Hydroxide
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HEMPVANA MAXIMUM STRENGTH PAIN RELIEF
trolamine salicylate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73287-022 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 EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM HYDROXIDE (UNII: 55X04QC32I) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) 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) PEG-100 STEARATE (UNII: YD01N1999R) STEARIC ACID (UNII: 4ELV7Z65AP) ALLANTOIN (UNII: 344S277G0Z) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HEXYLENE GLYCOL (UNII: KEH0A3F75J) DIMETHICONE (UNII: 92RU3N3Y1O) CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73287-022-01 1 in 1 CARTON 02/28/2022 1 71 g in 1 APPLICATOR; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/28/2022 Labeler - TELEBRANDS CORP (177266558) Establishment Name Address ID/FEI Business Operations Neutraderm, Inc. 146224444 manufacture(73287-022)

