DERMOPLAST PAIN RELIEVING- benzocaine, menthol spray 
Advantice Health

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Dermoplast Pain relieving Spray

Drug Facts

Active ingredients

Benzocaine 20%

Menthol 0.5%

Purpose

Topical analgesic

Uses

for temporary relief of pain and itching associated with • sunburn • insect bites • minor cuts • minor burns • minor skin irritations 

Warnings

For external use only

do not use near heat, flame, or fire or while smoking Flammable 

Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other "caine" anesthetics. Allergy alert:

When using this product

  • avoid contact with eyes. Do not spray in the face of mouth.
  • use only as directed
  • intentional misuse by deliberately concentrating or inhaling the contents can be harmful or fatal 
  • do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • itching, rash or irritation develops

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 to 4 times daily
 Children under 2 years of age  consult a doctor  

Other information

Inactive ingredients

acetylated lanoline alcohol, aloe vera gel (decolorized), butane, cetyl acetate, hydrofluorocarbon 152a, methylparaben, PEG-400 monolaurate, polysorbate 85

Questions?

Mon - Fri 8AM- 5PM EST 1-800-345-0032Dermoplast.com

Package Labeling:

Label

DERMOPLAST PAIN RELIEVING 
benzocaine, menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16864-690
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BUTANE (UNII: 6LV4FOR43R)  
CETYL ACETATE (UNII: 4Q43814HXS)  
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 85 (UNII: A7F3N56197)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16864-690-0178 g in 1 CAN; Type 0: Not a Combination Product03/18/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01703/18/2022
Labeler - Advantice Health (192527062)

Revised: 12/2023
Document Id: 0d12185e-8d41-7d76-e063-6294a90a2cf4
Set id: dad00c95-4e11-3eec-e053-2a95a90a7a18
Version: 2
Effective Time: 20231221
 
Advantice Health