FDA.reportPublic FDA data

FORMULA 4 PAIN

Manufacturer
Lifequest Creations LLC
Effective date
2023-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:31:46

Label at a glance#

ProductFORMULA 4 PAIN
Active ingredientLIDOCAINE HYDROCHLORIDE, MENTHOL, UNSPECIFIED FORM
Label structure7 sections

Indications and uses

Fast Pain Relief

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients                Purpose

Lidocaine HCl 4%                  Topical Anesthetic

Menthol 2%                          Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Fast Pain Relief

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY. NOT INTENDED FOR INGESTION DONT USE ONLARGE AREAS OF THE BODY OR ON CUT, IRRITATED OR SWOLLEN SKIN. Use only as directed, avoid contact with eyes and mucus membranes If pregnant or breast-feeding, ask a health care professional before use. If swallowed, get medical help

Direction

DOSAGE & ADMINISTRATION SECTION

Apply topically to area and rub in. Repeate as needed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Olive Oil, Shae Butter, Mango Butter, Hemp seed oil, Emulsifying wax, Stearic Acid, Palma rosa, Tea Tree, Eucalyptus, Camphor, Lavender, Ginger, Capsicum, Ale vera, Optiphen,  Arnica

Other information

SPL UNCLASSIFIED SECTION

Great for : Sore muscles, aching joints, gout flare-ups and body pain and other sports related pain.

Lidocaine helps alleviate stiffness, inflammation, joint pain, muscle soreness and more. Hemp seed oil allows ingredients to cross and absorb into

the skin. Menthol crystals gives instant cooling and pain releif. Physician formulated combined with other ingredients 4F pain cream is a great way

to control discomfort. Great before and after workouts.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58292-00358292-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
OLIVE OIL6UYK2W1W1EIACT
SHEA BUTTERK49155WL9YIACT
MANGOI629I3NR86IACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
PALMAROSA OIL0J3G3O53STIACT
TEA TREE OILVIF565UC2GIACT
EUCALYPTUS OIL2R04ONI662IACT
CAMPHOR (NATURAL)N20HL7Q941IACT
LAVENDER OILZBP1YXW0H8IACT
GINGER OILSAS9Z1SVUKIACT
CAPSICUM OLEORESINUW86K581WYIACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ARNICA MONTANA WHOLEO80TY208ZWIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
MENTHOL, UNSPECIFIED FORML7T10EIP3AACTIB

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
003c0182-8262-d37d-e063-6294a90af2ff433e2b4b-2add-4090-894e-38d82a8be5192023-07-11WarningsExact identifier
spl set id: 433e2b4b-2add-4090-894e-38d82a8be519

Reported adverse events (FAERS/openFDA)#

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