RES-Q ANALGESIC TOPICAL PAIN RELIEF- lidocaine hydrochloride liquid 
CONAIR CORPORATION

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Res-Q Analgesic Topical Pain Relief Spray

Res-Q Analgesic Topical Pain Relief Spray

Active Ingredient

Lidocaine Hydrochloride 4%

Purpose

Topical Analgesic

Uses:

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

Directions:

Adult use only: Shake well. Apply (spray) onto affected area not more than 3-4 times daily.

Inactive Ingredients:

Water, urea, isopropyl palmitate, PEG-8, Polysorbate 80, dimethicone, phenoxyethanol, sodium hydroxide, propylene glycol, allantoin, carbomer, cetrimonium bromide, diazolidinyl urea, lecithin, iodopropyl butylcarbamate.

Warnings

For external use only.

Stop use and consult a doctor immediately if you experience weakness; confusion; headache; difficulty breathing; pale, grey or blue-colored skin, lips, or nail beds or any other unusual symptoms.

Do not use more than the recommended dose.

Do not cover the treated area with a dressing or bandage.

Children should be closely observed during and after use of this product as they are at greater risk for serious side effects.

Do not use large quantities, particularly over raw surfaces or blistered areas.

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

Seek immediate medical attention if ingested.

Keep away from mouth and eyes.

If contact occurs, rinse thoroughly with water.

Keep away from children. Do not use on children under 14.

Res-Q Analgesic Topical Pain Relief Spray 2oz/60ml

SprayLabel
RES-Q ANALGESIC TOPICAL PAIN RELIEF 
lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12829-2001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
UREA (UNII: 8W8T17847W)  
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ALLANTOIN (UNII: 344S277G0Z)  
CETRIMONIUM BROMIDE (UNII: L64N7M9BWR)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:12829-2001-060 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/26/201412/19/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34802/26/201412/19/2016
Labeler - CONAIR CORPORATION (001661222)
Establishment
NameAddressID/FEIBusiness Operations
CSR Cosmetic Solutions Inc.243501959manufacture(12829-2001)

Revised: 12/2016
 
CONAIR CORPORATION