Pain Relief Roll On by Evora Worldwide / Inspec Solutions LLC Pain Releif Lidocaine 4%

Pain Relief Roll On by

Drug Labeling and Warnings

Pain Relief Roll On by is a Otc medication manufactured, distributed, or labeled by Evora Worldwide, Inspec Solutions LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PAIN RELIEF ROLL ON EVORA LABS- lidocaine liquid 
Evora Worldwide

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Pain Releif Lidocaine 4%

Active ingredient                                               Purpose

Lidocaine 4%..................................................... Topical analgesic

Uses

For temporary relief of pain and itching

Warnings

For externa use only.

When using this product use only as directed do not bandage tightly avoid contact with
eyes  do not apply to wounds or  damaged skin do not use in large quantities, particularly over raw  surface or blistered areas.

Stop use and ask doctor if condition worsens  symptoms persist for more than 7 days or clear up and occur again within a few days

Flammable keep away from fire or flame

If pregnant or breast-feeding, ask a health professional before
use.

Keep out of reach of children

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

Directions

Adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily
Children under 2 years old: consult a doctor

Inactive ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer
ALOE VERA LEAF
AMINOMETHYLPROPANOL 
Caprylyl Methicone
CETOSTEARYL ALCOHOL
CETETH-20 PHOSPHATE
DIHEXADECYL PHOSPHATE 
DIMETHICONE 
EDETATE DISODIUM
Ethylhexylglycerin 
GLYCERYL STEARATE
METHYLPARABEN 
SD ALCOHOL 40
STEARETH-21 
WATER

Questions?

1-888-793-8450

PAIN RELIEF ROLL ON  EVORA LABS
lidocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77375-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MYRISTYL TRISILOXANE (UNII: J7960S4R1T)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETETH-20 PHOSPHATE (UNII: 921FTA1500)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
DIMETHICONE (UNII: 92RU3N3Y1O)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
METHYLPARABEN (UNII: A2I8C7HI9T)
ALCOHOL (UNII: 3K9958V90M)
STEARETH-21 (UNII: 53J3F32P58)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77375-007-02	1 in 1 CARTON	12/22/2020
1		74 mL in 1 BOTTLE, PLASTIC; 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	12/22/2020	12/09/2025

Labeler - Evora Worldwide (081336028)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC		081030372	manufacture(77375-007)

Revised: 12/2025

Document Id: 45ffd56f-af98-fcbc-e063-6394a90a5a90

34390-5

Set id: 6694758f-4d71-4ca4-b1c2-dace8871bf6c

Version: 7

Effective Time: 20251215