LIDOPRO PAIN RELIEF- capsaicin and lidocaine ointment

LidoPro Pain Relief by

Drug Labeling and Warnings

LidoPro Pain Relief by is a Otc medication manufactured, distributed, or labeled by Preferred Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

• Capsicum annum fruit extract (capsaicin)
• Lidocaine HCL
• Menthol
• Methyl Salicylate

Purpose

• counterirritant
• anesthetic
• analgesic

Uses

For the temporary relief of joint pain and muscle pain associated with:

• arthritis
• simple backache
• muscle sprains
• muscle strains

Warnings

For external use only.

Do not use

• on damaged, irritated or infected skin
• with a bandage or heating pad
• if you are allergic to any ingredients in this product

When using this product

avoid contact with the eyes and mucous membranes

Stop use and ask doctor if

• condition worsens
• excessive skin
• irritation develops
• symptoms persist for more than 7 days
• symptoms clear up and occur again within 3 days

If pregnant or breast-feeding

ask a health professional before use.

Keep out of reach of children

If ingested, seek medical help or contact a Poison Control Center immediately.

Flammable

Keep away from excessive heat or open flame.

Directions

Adults and children 12 years of age and older:

• clean and dry the affected area
• apply product directly to skin, up to 4 times daily
• wash hands immediately after use

Children under 12 years of age: Consult physician.

Other information

• Store in a cool, dry place with lid tightly closed
• if the tamper-evident foil seal is not intact, do not use

Inactive ingredient

allantoin, aloe barbadensis leaf juice, ammonium acryloyldimethyltaurate/vp copolymer, cetyl alcohol, chamomilla recutita matricaria flower extract, dimethicone, disodium EDTA, ethylhexylglycerin, glycerin, glyceryl stearate, inulin lauryl carbamate, PEG-100 stearate, phenoxyethanol, stearic acid, triethanolamine, water

Questions?

(800) 224-2048 or info@clinicpharma.com

Relabeled By: Preferred Pharmaceuticals Inc.

NDC: 68788-8833-9

Label

INGREDIENTS AND APPEARANCE

LIDOPRO PAIN RELIEF 
capsaicin and lidocaine ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68788-8833(NDC:83881-001)
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, (+)- (UNII: C6B1OE8P3W) (MENTHOL, (+)- - UNII:C6B1OE8P3W)	MENTHOL, (+)-	10 mg  in 100 mg
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	4 mg  in 100 mg
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	27.5 mg  in 100 mg
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.0325 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PEG-100 MONOSTEARATE (UNII: YD01N1999R)
ALLANTOIN (UNII: 344S277G0Z)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68788-8833-9	1 in 1 BOX	02/21/2025
1		9900 mg in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/21/2025

Labeler - Preferred Pharmaceuticals Inc. (791119022)

Registrant - Preferred Pharmaceuticals Inc. (791119022)

Establishment
Name	Address	ID/FEI	Business Operations
Preferred Pharmaceuticals Inc.		791119022	RELABEL(68788-8833)