Label: HEMPVANA MAXIMUM STRENGTH PAIN RELIEF- trolamine salicylate lotion
- NDC Code(s): 73287-022-01
- Packager: TELEBRANDS CORP
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 28, 2022
If you are a healthcare professional or from the pharmaceutical industry 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 not final part348 02/28/2022 Labeler - TELEBRANDS CORP (177266558) Establishment Name Address ID/FEI Business Operations Neutraderm, Inc. 146224444 manufacture(73287-022)