FDA.reportPublic FDA data

Hempvana Pain Relief Gel Patch

Manufacturer
Telebrands Corp. | Foshan Aqua Gel Biotech Co., Ltd.,
Effective date
2021-05-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:44:23

Label at a glance#

ProductHempvana Pain Relief
Active ingredientLIDOCAINE
Label structure10 sections

Storage and handling

Avoid storing patches in direct sunlight. Protect patches from excessive moisture.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine (4%)

OTC - PURPOSE SECTION

Lidocaine (4%)..................................Topical Anesthetic

INDICATIONS & USAGE SECTION

For temporary pain relief

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use

  • more than one patch at a time
  • on wounds, cuts, damaged, broken and/or irritated skin
  • over raw surfaces or blistered areas
  • at the same time as other topical analgesics
  • if allergice to lidocaine or any inactive ingredients
  • if package is damaged or open

OTC - WHEN USING SECTION

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 heading pads) to the area of use
  • Avoid contact with eyes or mucous membranes

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Condition worsens
  • Symptoms persist for more than 7 days or clear up and occur again within a few days
  • Redness is present or irritation develops

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years of age

  • Clean and dry affected area
  • Follow application instructions above to apply patch to skin
  • Apply one patch to affected area no more than 3-4 times daily
  • Remove patch from affected area after meximum of 8 hours application
  • Children under 12 years of age: consult a doctor

STORAGE AND HANDLING SECTION

Avoid storing patches in direct sunlight. Protect patches from excessive moisture.

INACTIVE INGREDIENT SECTION

Dihydroxyaluminum Aminoacetate, Glycerin, Kaolin, Methylparaben, Polyacrylic Acid, Polysorbate 80, Povidone, Propylene Glycol, Propylparaben, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water

OTC - QUESTIONS SECTION

Call (855) 877-4503 (M-F, 9am-5pm EST)

DESCRIPTION SECTION

To Apply

  • Peel apart
  • Remove one side of film
  • Place on affected area
  • Remove remaining film
  • Press patch gently

Dist. by: Telebrands Corp. 79 Two Bridges Road, Fairfield, NJ 07004

For more information, visit www.Hempvana.com

*This Hempvana branded product does not contain any ingredients from the hemp plant.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 73287-002-01

Hempvana

#1 hemp brand on tv

PAIN RELIEF

Gel-Patch

Apply for 8 hours

MAXIMUM STRENGTH

UNSCENTED

For temporary, numbing pain relief

  • Back
  • Neck
  • Shoulders
  • Knees
  • Elbows

Lidocaine 4%

6 Patches

3.9" x 5.5" (10 cm x 14 cm) each

Pain PatchPain Patch

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73287-00273287-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
TARTARIC ACIDW4888I119HIACT
LIDOCAINE98PI200987ACTIB
DIHYDROXYALUMINUM AMINOACETATEDO250MG0W6IACT
GLYCERINPDC6A3C0OXIACT
METHYLPARABENA2I8C7HI9TIACT
POVIDONEFZ989GH94EIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PROPYLPARABENZ8IX2SC1OHIACT
WATER059QF0KO0RIACT
KAOLIN24H4NWX5COIACT
POLYACRYLIC ACID (250000 MW)9G2MAD7J6WIACT
POLYSORBATE 806OZP39ZG8HIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
TITANIUM DIOXIDE15FIX9V2JPIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c32f7570-41c5-9ae4-e053-2a95a90a85e094b8e1fe-5c96-c22b-e053-2a95a90aacaa2021-05-25WarningsExact identifier
spl id: c32f7570-41c5-9ae4-e053-2a95a90a85e0
spl set id: 94b8e1fe-5c96-c22b-e053-2a95a90aacaa

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.