LIDOPRO PAIN RELIEF- capsaicin and lidocaine ointment 
Advanced Rx of Tennessee, LLC

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LidoPro Ointment 99gm

Active ingredient

Purpose

Uses

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

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:

Children under 12 years of age: Consult physician.

Other information

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lidopro Ointment #99

LIDOPRO PAIN RELIEF 
capsaicin and lidocaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80425-0452(NDC:83881-001)
Route of AdministrationTRANSDERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, (+)- (UNII: C6B1OE8P3W) (MENTHOL, (+)- - UNII:C6B1OE8P3W) MENTHOL, (+)-10 mg  in 100 mg
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 mg  in 100 mg
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE27.5 mg  in 100 mg
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM) CAPSAICIN0.0325 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)  
TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
WATER (UNII: 059QF0KO0R)  
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
GLYCERYL STEARATE (UNII: 230OU9XXE4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PEG-100 STEARATE (UNII: YD01N1999R)  
ALLANTOIN (UNII: 344S277G0Z)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
INULIN LAURYL CARBAMATE (UNII: 48RFF58ESG)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80425-0452-11 in 1 BOX11/26/2024
19900 mg in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01711/26/2024
Labeler - Advanced Rx of Tennessee, LLC (117023142)
Establishment
NameAddressID/FEIBusiness Operations
Advanced Rx of Tennessee, LLC117023142repack(80425-0452)

Revised: 1/2025
Document Id: 2bc81112-204c-2514-e063-6394a90a80ed
Set id: 27d5997b-1cc2-41c2-e063-6394a90ac74a
Version: 2
Effective Time: 20250115
 
Advanced Rx of Tennessee, LLC