Physician Force Maximum Strength Pain Relief Cream

Manufacturer
Physician Force, LLC
Effective date
2020-09-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:51

Label at a glance#

ProductPhysician Force Maximum Strength Pain Relief
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

For the temporary relief of pain and itching associated with minor burns, sunburns, minor cuts, scrapes, insect bites or minor skin irritations.

Dosage and administration

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 physician.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine hydrochloride4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

  • For the temporary relief of pain and itching associated with minor burns, sunburns, minor cuts, scrapes, insect bites or minor skin irritations.

Warnings:

WARNINGS SECTION

For external use only. Not intended for ingestion

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with the eyes

Do not use

OTC - DO NOT USE SECTION

  • in large quantities, particularly over raw surfaces or blistered areas.

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms persist for more than seven days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

contact physician prior to use

Directions:

DOSAGE & ADMINISTRATION SECTION

  • 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 physician.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Acrylates Copolymer, Aloe Barbadensis leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Amica Montana Extract, Boswellia Serrata Extract, Cetyl Alcohol, Ethylhexylglycerin, IlexParaguayensis (Yerba Mate) Extract, isopropyl Myristate, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, Stearic Acid, Triethanolamine.

Other information:

SPL UNCLASSIFIED SECTION

  • Store at room temperature.

Questions?

OTC - QUESTIONS SECTION

(786) 456-4259 (Monday-Friday 9-5pm EST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80438-08180438-081-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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
074af059-5c0c-c02a-e063-6394a90a770aaee3c37a-71e5-b6e5-e053-2a95a90a6d8a2023-10-09WarningsExact identifier
spl set id: aee3c37a-71e5-b6e5-e053-2a95a90a6d8a

Reported adverse events (FAERS/openFDA)#

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