DCH PAIN RELIEF- lidocaine 4% spray 
Derma Care Research Labs, LLC

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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DCH Pain Relief Spray, Lidocaine 4%

Lidocaine 4%

External Analgesic.

For the temporary relief of pain and itching due to sunburn, minor burns, insect bites, minor cuts, scrapes, and minor skin irritations.

For external use only.

Flammable--Do not use while smoking or near heat or flame.

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

When using this product avoid contact with eyes. Rinse eyes with water to remove. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120F.

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

Keep out of reach of children. If the product is swallowed, get medical help or contact a Poison Control Center right away.

Adults and children 2 years and older: apply to the affected area, not more than 3 to 4 times a day. Children under 2 years of age: consult a physician. To apply to face, squeeze into palm of hand and gently apply.

Water, Glycerin, Alcohol Denat., Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Chamomilla Recutita (Matricaria) Flower Extract, Cucumis Sativus (Cucumber) Fruit Extract, Disodium EDTA, Triethanolamine, Diazolidinyl Urea, Simethicone.

Label

DCH PAIN RELIEF 
lidocaine 4% spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72839-226
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CUCUMBER (UNII: YY7C30VXJT)  
DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALCOHOL (UNII: 3K9958V90M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
TROLAMINE (UNII: 9O3K93S3TK)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CHAMOMILE (UNII: FGL3685T2X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72839-226-04113 g in 1 CAN; Type 0: Not a Combination Product06/10/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/10/2021
Labeler - Derma Care Research Labs, LLC (116817470)
Registrant - Derma Care Research Labs, LLC (116817470)
Establishment
NameAddressID/FEIBusiness Operations
Derma Care Research Labs116817470manufacture(72839-226)

Revised: 7/2023
Document Id: 00efda74-d433-04be-e063-6294a90a6d98
Set id: 00efda74-d434-04be-e063-6294a90a6d98
Version: 1
Effective Time: 20230720
 
Derma Care Research Labs, LLC