SUNBURNT PLUS- lidocaine hydrochloride gel 
Quest Products, LLC.

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SunBurnt ® PLUS

Drug Facts

Active Ingredient

Lidocaine Hydrochloride 4.0%

Purpose

External analgesic

Uses

Temporarily relieves pain and itching due to:

Warnings

For external use only

Do not use

  • in large quantities, particularly over raw surfaces or blistered areas
  • if you have an allergy or hypersensitivity to any ingredients

Ask a doctor before use if

  • you have severe sunburn
  • you have a rash or broken or compromised skin

When using this product

  • Avoid contact with eyes

Stop use and ask a doctor

  • condition worsens
  • symptoms last more than 7 days or clear up and occur again within a few days

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

Directions

Other Information

Inactive Ingredients

Water, Propanediol,Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Calunda Officinalis Extract, Cucumis Sativus (Cucumber) Seed Extract, Panthenol, Dimethyl Isosorbide, Caprylyl Glycol, Chlorophenesin, Phenoxyethanol, Sodium Hyaluronate, Tocopheryl Acetate

Questions or Comments?

Sunburnt.com

PRINCIPAL DISPLAY PANEL - 118mL Tube Carton

PDP

SUNBURNT PLUS 
lidocaine hydrochloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68229-600
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
PROPANEDIOL (UNII: 5965N8W85T)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
HYDROXYETHYL CELLULOSE (5500 MPA.S AT 2%) (UNII: M825OX60H9)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
PANTHENOL (UNII: WV9CM0O67Z)  
CUCUMBER SEED (UNII: BT3S9L53JK)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68229-600-011 in 1 CARTON07/01/2020
1NDC:68229-600-02118.294 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01707/01/2020
Labeler - Quest Products, LLC. (075402441)
Establishment
NameAddressID/FEIBusiness Operations
Fill Tech USA926433855manufacture(68229-600)

Revised: 11/2023
Document Id: 0a36e97f-6aba-7afa-e063-6394a90a1f02
Set id: 12de2559-05b0-4580-84c1-d3bd010b1c99
Version: 3
Effective Time: 20231115
 
Quest Products, LLC.