Vonaflex+ Effective Pain Relief Topical Analgesic

Vonaflex+ Effective Pain Relief Topical Analgesic
SPL v1
SPL
SPL Set ID 0901244a-7d41-413a-b424-92a807532f28
Route
TOPICAL
Published
Effective Date 2026-01-23
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Inactive Ingredients
Arnica Montana Whole Caramel Carbomer Homopolymer, Unspecified Type Cetostearyl Alcohol Cetyl Esters Wax Edetate Disodium Diethylene Glycol Monoethyl Ether Ethyl Macadamiate Ethylhexylglycerin Glycerin Sunflower Oil Menthyl Lactate, (-)- Polyoxyl 40 Hydrogenated Castor Oil Phenoxyethanol Propylene Glycol Scutellaria Baicalensis Root Tetrahydrodiferuloylmethane .alpha.-tocopherol Acetate Trolamine Water

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH DRUG Active Since 2025-12-23

Description

Lidocaine hydrochloride 4%

Purpose

Topical Analgesic


Medication Information

Purpose

Topical Analgesic

Description

Lidocaine hydrochloride 4%

Uses:
  • For temporary relief of pain
Warnings:

For external use only

Do Not Use
  • in large quantities, particularly over raw surfaces or blistered areas
Drug Facts

Directions:
  • Adults and children 2 years of age and older: Apply a thin layer to the affected area and massage until the lotion is no longer visible,  up to three times a day.
  • Children under 2 years of age: consult a doctor.
Package Labeling:

Active Ingredients

Lidocaine hydrochloride 4%

Other Information:
  • Store at 20-25°C (68-77°F) and protect from moisture
Inactive Ingredients:

Arnica Montana Extract, Caramel, Carbomer, Cetearyl Alcohol, Cetyl Esters, Disodium EDTA, Ethoxydiglycol, Ethyl Macadamiate, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Angustifolia (Lavender) Flower Oil, Menthyl Lactate, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Propylene Glycol, Scutellaria Baicalensis Root Extract, Tetrahydrodiferuloylmethane, Tocopheryl Acetate, Triethanolamine, Water (Aqua)

When Using This Product
  • Avoid contact with the eyes
Stop Use and Ask A doctor If
  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
If Pregnant Or Breast Feeding,

ask a health professional before use.

Keep Out of Reach Of children.

If swallowed, get medical help or contact a Poison Control Center right away.


Structured Label Content

Uses:
  • For temporary relief of pain
Purpose

Topical Analgesic

Warnings:

For external use only

Do Not Use (Do not use)
  • in large quantities, particularly over raw surfaces or blistered areas
Drug Facts

Directions:
  • Adults and children 2 years of age and older: Apply a thin layer to the affected area and massage until the lotion is no longer visible,  up to three times a day.
  • Children under 2 years of age: consult a doctor.
Package Labeling:

Active Ingredients (Active ingredients)

Lidocaine hydrochloride 4%

Other Information: (Other information:)
  • Store at 20-25°C (68-77°F) and protect from moisture
Inactive Ingredients: (Inactive ingredients:)

Arnica Montana Extract, Caramel, Carbomer, Cetearyl Alcohol, Cetyl Esters, Disodium EDTA, Ethoxydiglycol, Ethyl Macadamiate, Ethylhexylglycerin, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Angustifolia (Lavender) Flower Oil, Menthyl Lactate, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Propylene Glycol, Scutellaria Baicalensis Root Extract, Tetrahydrodiferuloylmethane, Tocopheryl Acetate, Triethanolamine, Water (Aqua)

When Using This Product (When using this product)
  • Avoid contact with the eyes
Stop Use and Ask A doctor If (Stop use and ask a doctor if)
  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.
If Pregnant Or Breast Feeding, (If pregnant or breast-feeding,)

ask a health professional before use.

Keep Out of Reach Of children. (Keep out of reach of children.)

If swallowed, get medical help or contact a Poison Control Center right away.


Advanced Ingredient Data


Raw Label Data

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