FDA.reportPublic FDA data

VigorWell Neuropathy Cream

Manufacturer
Shenzhen Situya Trading Co., Ltd.
Effective date
2023-05-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:30:48

Label at a glance#

ProductVigorWell Neuropathy Cream
Active ingredientTHYMOL, MENTHOL, CAMPHOR (SYNTHETIC)
Label structure12 sections

Dosage and administration

Apply this cream to the affected area. a Massage thoroughly for 30 seconds or until fully absorbed. UseQ cream sparingly initially and then apply as needed.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

MENTHOL 0.5%
CAMPHOR (SYNTHETIC) 0.5%
THYMOL 0.5%

Purpose

OTC - PURPOSE SECTION

Skin Conditione

Use

INDICATIONS & USAGE SECTION

Helpful as an aid to treat the symptoms of molluscum contagiosum.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on iritated skin on any area that is infected or reddened a Do not use it if pregnant or if there is any allergic
reaction to this product Avoid contact with eyes.

Stop Use

OTC - STOP USE SECTION

if discomfort persists

Ask Doctor

OTC - ASK DOCTOR SECTION

if you have diabetes or poor blood circulation

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

lf product gets into eyes, flush with water for 15 minutes m lf swallowed, get medical help or contact a Poison
Control Center riaht awav

Directions

DOSAGE & ADMINISTRATION SECTION

Apply this cream to the affected area. a Massage thoroughly for 30 seconds or until fully absorbed. UseQ
cream sparingly initially and then apply as needed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

GLYCERIN
LIQUID PETROLEUM
WATER
ALCOHOL

Questions

OTC - QUESTIONS SECTION

Deosperavi LLC
426W Fir Rd #1057
Carthage,MO 64836
www.ivigorwell.com
service@ivigorwell.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0101

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82739-011-012024-01-30C16284748780-11030e365-60fe-111a-e063-dadaa90a10e282739-011-01

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82739-01182739-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
THYMOL3J50XA376EACTIB
MENTHOLL7T10EIP3AACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
LIQUID PETROLEUM6ZAE7X688JIACT
WATER059QF0KO0RIACT

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
29ead96f-98f6-7f70-e063-6294a90aaecafc94abd8-0a44-6546-e053-6394a90a8a0d2024-12-23WarningsExact identifier
spl set id: fc94abd8-0a44-6546-e053-6394a90a8a0d

Reported adverse events (FAERS/openFDA)#

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