FDA.reportPublic FDA data

Workvie

Manufacturer
Marketites LLC
Effective date
2025-10-29
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:41:29

Label at a glance#

ProductWorkvie
Active ingredientMENTHOL, LIDOCAINE HYDROCHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Lidocaine HCL 4% w/w

Menthol 1% w/w

OTC - PURPOSE SECTION

Purpose

Topical analgesic

Topical analgesic

INDICATIONS & USAGE SECTION

USES For temporary relief of pain.

WARNINGS SECTION

Warnings

For external use only. Avoid contact with eyes.

OTC - DO NOT USE SECTION

Do not use in large quantities, particularly over raw surfaces, or blistered areas.

OTC - ASK DOCTOR SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

If pregnant or breast feeding, ask a health professional.

DOSAGE & ADMINISTRATION SECTION

Directions adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.

Children under 2 years of age: consult a doctor.

OTHER SAFETY INFORMATION

Other Information

store in a cool dry place between (59-86°F) 15-30°C

don't use if seal over cap is broken, torn or missing

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Arnica Extract, Bromelain, C13-14 Isoparaffin, Caprylyl Glycol, Capsicum Annuum Fruit Extract, Chamomile Extract, Devil’s Claw Extract, Dimethicone, Dimethyl Sulfone (MSM), Eucalyptus Oil, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Glycol Stearate, Horse Chestnut Extract, Isopropyl Myristate, Laureth-7, Lemon Balm Extract, Linden Flower Extract, Menthyl Lactate, PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Rosemary Extract, Sweet Almond Oil, Water, Willow Bark Extract

OTC - QUESTIONS SECTION

Questions or comments

info@workvie.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Workvie Lidocaine Pain Relieving Roll On LotionWorkvie Lidocaine Pain Relieving Roll On Lotion

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1595624lidocaine HCl 4 % / menthol 1 % Topical CreamPSN6
2049723Workvie 4 % / 1 % Roll On Topical CreamPSN6
2049723lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML Topical Cream [Workvie]SBD6
1595624lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML Topical CreamSCD6
1595624lidocaine hydrochloride 4 % / menthol 1 % Topical CreamSY6
2049723Workvie Roll On Analgesic (lidocaine HCl 4 % / menthol 1 % ) Topical CreamSY6

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130661646159110GTIN-13: 0661646159110
EAN-13: 0661646159110
GTIN-12: 661646159110
UPC-A: 661646159110
GTIN storage (14 digits): 00661646159110		FDA Lidocaine Lotion 2021.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72393-203-25Workvie71 g in 1 BOTTLE, WITH APPLICATORCREAM716
72393-203-42Workvie284 g in 1 BOTTLE, WITH APPLICATORCREAM2846
72393-203-62Workvie426 g in 1 BOTTLE, WITH APPLICATORCREAM4266

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72393-20372393-203-25, 72393-203-62, 72393-203-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
GLYCOL STEARATE0324G66D0EIACT
HORSE CHESTNUT3C18L6RJAZIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
PEG-100 STEARATEYD01N1999RIACT
ARNICA MONTANAO80TY208ZWIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CHAMOMILEFGL3685T2XIACT
ROSEMARY OIL8LGU7VM393IACT
ALOE VERA LEAFZY81Z83H0XIACT
LEMON BALM OILMJ76269K9SIACT
LINDEN LEAFRU6O456OJ1IACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SALIX NIGRA BARKQU52J3A5B3IACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
GLUCOSAMINE SULFATE POTASSIUM CHLORIDE15VQ11I66NIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
MENTHYL LACTATE, (-)-2BF9E65L7IIACT
ALMOND OIL66YXD4DKO9IACT
HARPAGOPHYTUM PROCUMBENS ROOT1OYM338E89IACT
MENTHOLL7T10EIP3AACTIB
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
C13-14 ISOPARAFFINE4F12ROE70IACT
FRUIT BROMELAINF0ZCA6O9QTIACT
DIMETHICONE92RU3N3Y1OIACT
CAPSICUM ANNUUM WHOLE7FKZ3QQQ1FIACT
POLYACRYLAMIDE (10000 MW)E2KR9C9V2IIACT
LAURETH-7Z95S6G8201IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-05-28full-release2026-06-01 01:01:51

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
WorkvieLIDOCAINE HCL, MENTHOLMarketites LLCaebaffb5-58dd-ebd5-e053-2a95a90a14ed2025-10-29WarningsExact identifier
ndc (package): 72393-203-62
ndc (package): 72393-203-42
ndc (package): 72393-203-25
ndc (product): 72393-203
ndc11 (package): 72393020325
ndc11 (package): 72393020362
ndc11 (package): 72393020342
spl id: 424ff45b-890a-55ad-e063-6294a90a4f99
spl set id: aebaffb5-58dd-ebd5-e053-2a95a90a14ed

Reported adverse events (FAERS/openFDA)#

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