Physician Force Maximum Strength Pain Relief Cream

Physician Force Maximum Strength Pain Relief by

Drug Labeling and Warnings

Physician Force Maximum Strength Pain Relief by is a Otc medication manufactured, distributed, or labeled by Physician Force, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PHYSICIAN FORCE MAXIMUM STRENGTH PAIN RELIEF- lidocaine hydrochloride cream 
Physician Force, LLC

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Physician Force Maximum Strength Pain Relief Cream

Drug Facts

Active ingredients

Lidocaine hydrochloride4%

Purpose

Topical Analgesic

Uses:

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

Warnings:

For external use only. Not intended for ingestion

When using this product

• Avoid contact with the eyes

Do not use

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

Stop use and ask a doctor if

symptoms persist for more than seven days.

Keep out of reach of children.

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

If pregnant or breast-feeding,

contact physician prior to use

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 physician.

Inactive ingredients:

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:

• Store at room temperature.

Questions?

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

Package Labeling:

PHYSICIAN FORCE MAXIMUM STRENGTH PAIN RELIEF 
lidocaine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80438-081
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
CETYL ALCOHOL (UNII: 936JST6JCN)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
STEARIC ACID (UNII: 4ELV7Z65AP)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80438-081-00	113.4 g in 1 JAR; Type 0: Not a Combination Product	09/10/2020	12/30/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/10/2020	12/30/2022

Labeler - Physician Force, LLC (117593205)

Revised: 10/2023

Document Id: 074af059-5c0c-c02a-e063-6394a90a770a

34390-5

Set id: aee3c37a-71e5-b6e5-e053-2a95a90a6d8a

Version: 2

Effective Time: 20231009