NDC 36800-883

Sunburn Pain relief

Lidocaine Hydrochloride 0.5%

Sunburn Pain relief is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Top Care. The primary component is Lidocaine Hydrochloride.

Product ID36800-883_3b45baff-4756-4895-b9df-486b605665a0
NDC36800-883
Product TypeHuman Otc Drug
Proprietary NameSunburn Pain relief
Generic NameLidocaine Hydrochloride 0.5%
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2016-02-12
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart348
Labeler NameTop Care
Substance NameLIDOCAINE HYDROCHLORIDE
Active Ingredient Strength1 g/100mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 36800-883-06

1 BOTTLE in 1 CARTON (36800-883-06) > 237 mL in 1 BOTTLE
Marketing Start Date2016-02-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36800-883-06 [36800088306]

Sunburn Pain relief GEL
Marketing CategoryOTC monograph not final
Application Numberpart348
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-12
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LIDOCAINE HYDROCHLORIDE.5 g/100mL

OpenFDA Data

SPL SET ID:caf83b63-604e-43ae-85a0-b31db5fd2388
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1011849
  • UPC Code
  • 0036800663671
  • NDC Crossover Matching brand name "Sunburn Pain relief" or generic name "Lidocaine Hydrochloride 0.5%"

    NDCBrand NameGeneric Name
    36800-883Sunburn Pain reliefLidocaine Hydrochloride 0.5%
    0363-3192Aloe Gel Pain RelieverLidocaine Hydrochloride 0.5%
    11822-7782Burn relief aloeLidocaine Hydrochloride 0.5%
    69842-840Sunburn Pain RelieverLidocaine Hydrochloride 0.5%

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.