Label: HEMPVANA MAXIMUM STRENGTH PAIN RELIEF TOPICAL ANESTHETIC- lidocaine cream
- NDC Code(s): 73287-026-01
- Packager: Telebrands Corp
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 20, 2023
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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
- do not exceed the recommended daily dosage unless directed by a doctor.
- use only as directed. Read and follow all directions and warnings on this label.
- do not put this product into the rectum by using finger or any mechanical device or applicator.
Stop use and ask a doctor if
- condition worsens or does not improve within 7 days
- in case of bleeding
- symptom being treated does not subside or if redness, irritation, sweeling, pain, or other symptoms develop or increase. Certain persons can develop allergic reactions to ingredients in this product.
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Directions
- Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toilet tissue or a soft cloth, before application of this product to affected area.
- Apply to the affected area up to 6 times a day
- Children under 12 years of age: consult a doctor.
- Other information
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Inactive ingredients
Water/Aqua/Eau, Ethylhexyl Stearate, Butylene Glycol, Dimethicone, Stearic Acid, Caprylic/Capric Triglyceride, Cannabis Saliva (Hemp) Seed Oil, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Curcuma Longa (Turmeric) Root Extract, Allantoin, Glycerin, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Sodium Hydroxide, Disodium EDTA
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INGREDIENTS AND APPEARANCE
HEMPVANA MAXIMUM STRENGTH PAIN RELIEF TOPICAL ANESTHETIC
lidocaine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73287-026 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE 5 g in 100 g Inactive Ingredients Ingredient Name Strength CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TURMERIC (UNII: 856YO1Z64F) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ALLANTOIN (UNII: 344S277G0Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) SUNFLOWER SEED (UNII: R9N3379M4Z) WATER (UNII: 059QF0KO0R) STEARIC ACID (UNII: 4ELV7Z65AP) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5) HEXYLENE GLYCOL (UNII: KEH0A3F75J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73287-026-01 1 in 1 CARTON 02/17/2023 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 final M015 02/17/2023 Labeler - Telebrands Corp (177266558) Establishment Name Address ID/FEI Business Operations Neutraderm, Inc. 146224444 manufacture(73287-026)
