DERMOPLAST PAIN RELIEVING- benzocaine and levomenthol spray 
Advantice Health, LLC

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Dermoplast ®Pain Relieving

Drug Facts

Active ingredientsPurpose
Benzocaine 20%Topical analgesic
Menthol 0.5%Topical analgesic

Uses

for temporary relief of pain and itching associated with

Warnings

For external use only

Flammabledo not use near heat, flame, or fire or while smoking

Allergy alert

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

When using this product

  • avoid contact with eyes. Do not spray in the face or 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 olderapply to affected area not more than 3 to 4 times daily
Children under 2 years of ageconsult a doctor

Other information

Inactive ingredients

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

Questions?

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

Distributed by Advantice Health, LLC
Cedar Knolls, NJ 07927

PRINCIPAL DISPLAY PANEL - 78 g Can Label

Dermoplast®
Pain Relieving Spray

HOSPITAL STRENGTH

PAIN, BURN
& ITCH

RELIEVES PAIN FROM:
Minor Cuts & Scrapes, Burns,
Sunburns and Bug Bites

Fast Itch & Burn Relief

Provides Fast
Pain Relief

Cools and
Comforts

Soothing Aloe
& Lanolin

NET WT. 2.75 oz (78 g)

PRINCIPAL DISPLAY PANEL - 78 g Can Label
DERMOPLAST PAIN RELIEVING 
benzocaine and levomenthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:16864-680
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 g
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL5 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PEG-8 LAURATE (UNII: 762O8IWA10)  
POLYSORBATE 85 (UNII: A7F3N56197)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)  
CETYL ACETATE (UNII: 4Q43814HXS)  
BUTANE (UNII: 6LV4FOR43R)  
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:16864-680-0178 g in 1 CAN; Type 0: Not a Combination Product01/01/2014
2NDC:16864-680-0256 g in 1 CAN; Type 0: Not a Combination Product01/01/201412/31/2023
3NDC:16864-680-0385 g in 1 CAN; Type 0: Not a Combination Product01/01/2014
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/01/2014
Labeler - Advantice Health, LLC (192527062)

Revised: 12/2024
Document Id: 29147ec9-a0e6-1a10-e063-6394a90a44f7
Set id: 2347f0b8-d463-422d-8583-65624d9a1a91
Version: 6
Effective Time: 20241212
 
Advantice Health, LLC